RAD51, RAD51 recombinase, 5888

N. diseases: 363; N. variants: 16
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801321
rs1801321
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0476089
Disease:
Endometrial Carcinoma
0.010 GeneticVariation BEFREE This report describes studies of the distribution of genotypes and the frequency of alleles of the G135C (rs1801320) and G172T (rs1801321) RAD51 polymorphism in 630 paraffin-embedded samples of tumor tissue from patients with endometrial cancer. 24930116 2014
dbSNP: rs1801321
rs1801321
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE The aim of the present study was to evaluate the relationship between prostate cancer risk and the presence of single nucleotide polymorphisms (SNPs) in the genes involved in HRR, that is, RAD51 (rs1801320 and rs1801321), RAD51B (rs10483813 and rs3784099), XRCC2 (rs3218536), and XRCC3 (rs861539). 26339569 2015
dbSNP: rs1801321
rs1801321
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0600139
Disease:
Prostate carcinoma
0.010 GeneticVariation BEFREE The aim of the present study was to evaluate the relationship between prostate cancer risk and the presence of single nucleotide polymorphisms (SNPs) in the genes involved in HRR, that is, RAD51 (rs1801320 and rs1801321), RAD51B (rs10483813 and rs3784099), XRCC2 (rs3218536), and XRCC3 (rs861539). 26339569 2015
dbSNP: rs1801321
rs1801321
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0007137
Disease:
Squamous cell carcinoma
0.010 GeneticVariation BEFREE Combined effects of RAD51 (rs1801320 and rs1801321) and XRCC3 (rs861539) SNPs with environmental carcinogens (tobacco and alcohol) are associated with oral and oropharyngeal SCC development. 30033552 2019
dbSNP: rs1801321
rs1801321
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0007103
Disease:
Malignant neoplasm of endometrium
0.010 GeneticVariation BEFREE This report describes studies of the distribution of genotypes and the frequency of alleles of the G135C (rs1801320) and G172T (rs1801321) RAD51 polymorphism in 630 paraffin-embedded samples of tumor tissue from patients with endometrial cancer. 24930116 2014
dbSNP: rs1801321
rs1801321
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Our results underscored the existence of an association between XRCC3-5'-UTR-A/G (rs1799794) and RAD51-5'-UTR G172T (rs1801321) genotypes and BC risk in an Italian population. 28315507 2017
dbSNP: rs1801321
rs1801321
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE This report describes studies of the distribution of genotypes and the frequency of alleles of the G135C (rs1801320) and G172T (rs1801321) RAD51 polymorphism in 630 paraffin-embedded samples of tumor tissue from patients with endometrial cancer. 24930116 2014
dbSNP: rs1801321
rs1801321
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Our results underscored the existence of an association between XRCC3-5'-UTR-A/G (rs1799794) and RAD51-5'-UTR G172T (rs1801321) genotypes and BC risk in an Italian population. 28315507 2017
dbSNP: rs2412546
rs2412546
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The results showed that one SNP (rs2380165) in BLM and two (rs2412546 and rs4417527) in RAD51 were associated with breast cancer risk. 18974064 2009
dbSNP: rs2412546
rs2412546
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The results showed that one SNP (rs2380165) in BLM and two (rs2412546 and rs4417527) in RAD51 were associated with breast cancer risk. 18974064 2009
dbSNP: rs2928140
rs2928140
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE The aim of our study was to investigate single nucleotide polymorphisms (SNPs) in <i>RAD51</i> (rs2619679, rs2928140, and rs5030789) and <i>XRCC3</i> (rs1799796) involved in DNA double-strand break repair and their relationship to prostate cancer. 31186630 2019
dbSNP: rs2928140
rs2928140
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0600139
Disease:
Prostate carcinoma
0.010 GeneticVariation BEFREE The aim of our study was to investigate single nucleotide polymorphisms (SNPs) in <i>RAD51</i> (rs2619679, rs2928140, and rs5030789) and <i>XRCC3</i> (rs1799796) involved in DNA double-strand break repair and their relationship to prostate cancer. 31186630 2019
dbSNP: rs4417527
rs4417527
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The results showed that one SNP (rs2380165) in BLM and two (rs2412546 and rs4417527) in RAD51 were associated with breast cancer risk. 18974064 2009
dbSNP: rs4417527
rs4417527
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus
0.010 GeneticVariation BEFREE The genotype frequencies of rs1801320, rs4144242 and rs4417527 in patients with ESCC demonstrated no significant differences from those in control group (P>0.05). 24568492 2014
dbSNP: rs4417527
rs4417527
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The results showed that one SNP (rs2380165) in BLM and two (rs2412546 and rs4417527) in RAD51 were associated with breast cancer risk. 18974064 2009
dbSNP: rs5030789
rs5030789
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0600139
Disease:
Prostate carcinoma
0.010 GeneticVariation BEFREE A significant association was detected between <i>RAD51</i> rs5030789 polymorphism and <i>XRCC3</i> rs1799796 polymorphism and an increased risk of prostate cancer. 31186630 2019
dbSNP: rs5030789
rs5030789
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE A significant association was detected between <i>RAD51</i> rs5030789 polymorphism and <i>XRCC3</i> rs1799796 polymorphism and an increased risk of prostate cancer. 31186630 2019
dbSNP: rs7180135
rs7180135
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0280313
Disease:
Squamous cell carcinoma of oropharynx
0.010 GeneticVariation BEFREE These findings support significant roles of BRCA1 rs12516 and RAD51 rs7180135 in modifying the risk of recurrence of SCCOP, particularly HPV16-positive SCCOP. 28646528 2017
dbSNP: rs752492487
rs752492487
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C3463824
Disease:
MYELODYSPLASTIC SYNDROME
0.010 GeneticVariation BEFREE The GSTP1-Ile105Val polymorphism is likely to influence MDS risk and prognosis. 19027952 2009
dbSNP: rs1057519413
rs1057519413
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0432072
Disease:
Dysmorphic features
A 0.700 CausalMutation CLINVAR Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases. 24808016 2014
dbSNP: rs1057519413
rs1057519413
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0432072
Disease:
Dysmorphic features
A 0.700 CausalMutation CLINVAR A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination. 26253028 2015
dbSNP: rs1057519413
rs1057519413
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0432072
Disease:
Dysmorphic features
A 0.700 CausalMutation CLINVAR Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations. 25813273 2015
dbSNP: rs1555429623
rs1555429623
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C3281089
Disease:
MIRROR MOVEMENTS 2
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C4551570
Disease:
2-3 toe syndactyly
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0003466
Disease:
Anus, Imperforate
A 0.700 GeneticVariation CLINVAR