Source: CLINVAR

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: rs1057520009
rs1057520009
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057520009
rs1057520009
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057520009
rs1057520009
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.700 1.000 1 2016 2016
dbSNP: rs1057520009
rs1057520009
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057520009
rs1057520009
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
0.700 1.000 1 2016 2016
dbSNP: rs1057520010
rs1057520010
0.882 0.200 2 61492336 missense variant T/A;G snv
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
0.700 1.000 1 2016 2016
dbSNP: rs1057520010
rs1057520010
0.882 0.200 2 61492336 missense variant T/A;G snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057520010
rs1057520010
0.882 0.200 2 61492336 missense variant T/A;G snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057520010
rs1057520010
0.882 0.200 2 61492336 missense variant T/A;G snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057520010
rs1057520010
0.882 0.200 2 61492336 missense variant T/A;G snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.700 1.000 1 2016 2016