rs1057519900, FGFR2

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.882 0.120 10 121515259 missense variant C/T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.882 0.120 10 121515259 missense variant C/T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.882 0.120 10 121515259 missense variant C/T snv 0.700 1.000 1 2016 2016