rs121913474, FGFR2

N. diseases: 9
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 0.790 0.200 10 121515260 missense variant A/G snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.790 0.200 10 121515260 missense variant A/G snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.790 0.200 10 121515260 missense variant A/G snv 0.700 1.000 1 2016 2016
Craniofacial Dysostosis
CUI: C0010273
Disease: Craniofacial Dysostosis
29 0.790 0.200 10 121515260 missense variant A/G snv 0.010 1.000 1 2019 2019
Craniofacial dysostosis type 1
CUI: C2931196
Disease: Craniofacial dysostosis type 1
52 0.790 0.200 10 121515260 missense variant A/G snv 0.010 1.000 1 2019 2019
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.790 0.200 10 121515260 missense variant A/G snv 0.010 1.000 1 2019 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.790 0.200 10 121515260 missense variant A/G snv 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.790 0.200 10 121515260 missense variant A/G snv 0.010 1.000 1 2017 2017
Solid/Multicystic Ameloblastoma
CUI: C1513734
Disease: Solid/Multicystic Ameloblastoma
10 0.790 0.200 10 121515260 missense variant A/G snv 0.010 1.000 1 2019 2019