Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10849478
rs10849478
Entrez Id: 9918
Gene Symbol: NCAPD2
NCAPD2
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs11064237
rs11064237
Entrez Id: 9918
Gene Symbol: NCAPD2
NCAPD2
CUI: C0200635
Disease:
Lymphocyte Count measurement
0.700 GeneticVariation GWASDB The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes. 22286170 2012
dbSNP: rs714775
rs714775
Entrez Id: 9918;692148
Gene Symbol: NCAPD2;SCARNA10
NCAPD2;SCARNA10
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE <b>Results:</b> Three SNPs were significantly associated with survival of patients with colorectal cancer after correction for multiple testing, and two of the SNPs (<i>hsa-mir-196a-2</i> rs11614913 and <i>U85</i> rs714775) remained significant in multivariate analyses. 29483812 2018
dbSNP: rs714775
rs714775
Entrez Id: 9918;692148
Gene Symbol: NCAPD2;SCARNA10
NCAPD2;SCARNA10
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE <b>Results:</b> Three SNPs were significantly associated with survival of patients with colorectal cancer after correction for multiple testing, and two of the SNPs (<i>hsa-mir-196a-2</i> rs11614913 and <i>U85</i> rs714775) remained significant in multivariate analyses. 29483812 2018
dbSNP: rs2072374
rs2072374
Entrez Id: 9918
Gene Symbol: NCAPD2
NCAPD2
CUI: C3160718
Disease:
PARKINSON DISEASE, LATE-ONSET
0.010 GeneticVariation BEFREE The frequencies of the T allele of rs7311174 and the C allele of rs2072374 were significantly associated with late-onset Parkinson's disease (p = 0.048 and p = 0.044, respectively). 25166511 2014
dbSNP: rs7311174
rs7311174
Entrez Id: 9918
Gene Symbol: NCAPD2
NCAPD2
CUI: C3160718
Disease:
PARKINSON DISEASE, LATE-ONSET
0.010 GeneticVariation BEFREE The frequencies of the T allele of rs7311174 and the C allele of rs2072374 were significantly associated with late-onset Parkinson's disease (p = 0.048 and p = 0.044, respectively). 25166511 2014
dbSNP: rs758739
rs758739
Entrez Id: 9918
Gene Symbol: NCAPD2
NCAPD2
CUI: C0033860
Disease:
Psoriasis
0.010 GeneticVariation BEFREE We confirmed four known psoriasis susceptibility loci (IL12B, IFIH1, ERAP1 and RNF114; 2.30 × 10(-20)≤P≤2.41 × 10(-7)) and identified three new susceptibility loci: 4q24 (NFKB1) at rs1020760 (P=2.19 × 10(-8)), 12p13.3 (CD27-LAG3) at rs758739 (P=4.08 × 10(-8)) and 17q12 (IKZF3) at rs10852936 (P=1.96 × 10(-8)). 25006012 2014
dbSNP: rs740850
rs740850
Entrez Id: 9918
Gene Symbol: NCAPD2
NCAPD2
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE When the two family datasets were examined, none of the SNPs were significant in NE families, but two SNPs were associated with AD in Caribbean Hispanics: rs740850 in NCAPD2 (p = 0.0097) and rs1060620 in GAPDH (p = 0.042). 18340469 2008