Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.030 1.000 3 2016 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.020 1.000 2 2018 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2014 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.020 1.000 2 2018 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2014 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.020 1.000 2 2015 2019
dbSNP: rs147574894
rs147574894
0.925 0.080 4 102600911 missense variant A/G snv 9.6E-05 3.9E-04
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs147574894
rs147574894
0.925 0.080 4 102600911 missense variant A/G snv 9.6E-05 3.9E-04
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2019 2019
dbSNP: rs147574894
rs147574894
0.925 0.080 4 102600911 missense variant A/G snv 9.6E-05 3.9E-04
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2019 2019
dbSNP: rs147574894
rs147574894
0.925 0.080 4 102600911 missense variant A/G snv 9.6E-05 3.9E-04
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs148626207
rs148626207
4 102612593 missense variant T/C snv 8.0E-06 1.4E-05
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2019 2019
dbSNP: rs1598859
rs1598859
0.925 0.080 4 102585287 intron variant T/C snv 0.34
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs1598859
rs1598859
0.925 0.080 4 102585287 intron variant T/C snv 0.34
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2019 2019
dbSNP: rs1598859
rs1598859
0.925 0.080 4 102585287 intron variant T/C snv 0.34
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs1598859
rs1598859
0.925 0.080 4 102585287 intron variant T/C snv 0.34
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
0.010 1.000 1 2019 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.010 1.000 1 2019 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 1.000 1 2019 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.010 1.000 1 2019 2019
dbSNP: rs28362491
rs28362491
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2019 2019
dbSNP: rs3774934
rs3774934
0.851 0.080 4 102506319 intron variant A/C;G;T snv
Respiratory Distress Syndrome, Adult
0.010 1.000 1 2019 2019
dbSNP: rs3774937
rs3774937
0.776 0.280 4 102513096 intron variant T/C snv 0.26
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs3774937
rs3774937
0.776 0.280 4 102513096 intron variant T/C snv 0.26
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2019 2019