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: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
Adenoid Cystic Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
Transitional cell carcinoma of bladder
0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
0.776 0.200 3 179234284 missense variant A/G;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016