rs387906678, FGFR2

N. diseases: 5
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.
BENT BONE DYSPLASIA SYNDROME
CUI: C3281247
Disease: BENT BONE DYSPLASIA SYNDROME
10 0.851 0.120 10 121515263 missense variant A/C;G snv 0.800 1.000 1 2012 2012
Endometrial Neoplasms
CUI: C0014170
Disease: Endometrial Neoplasms
32 0.851 0.120 10 121515263 missense variant A/C;G snv 0.700 1.000 1 2014 2014
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.851 0.120 10 121515263 missense variant A/C;G snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.851 0.120 10 121515263 missense variant A/C;G snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.851 0.120 10 121515263 missense variant A/C;G snv 0.700 1.000 1 2016 2016