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: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial
0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
0.776 0.240 3 179203761 missense variant T/C;G snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.700 0