Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519044
rs1057519044
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs121913478
rs121913478
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		C 0.700 CausalMutation CLINVAR

dbSNP: rs121918487
rs121918487
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121918491
rs121918491
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121918505
rs121918505
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1434545235
rs1434545235
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1554927408
rs1554927408
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs77543610
rs77543610
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		C 0.700 CausalMutation CLINVAR

dbSNP: rs79184941
rs79184941
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		C 0.700 CausalMutation CLINVAR