Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913475

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913475(A;G)
Make rs121913475(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121519989
GeneFGFR2
is asnp
is mentioned by
dbSNPrs121913475
dbSNP (old)rs121913475
ClinGenrs121913475
ebirs121913475
HLIrs121913475
Exacrs121913475
Gnomadrs121913475
Varsomers121913475
Maprs121913475
PheGenIrs121913475
Biobankrs121913475
1000 genomesrs121913475
hgdprs121913475
ensemblrs121913475
gopubmedrs121913475
geneviewrs121913475
scholarrs121913475
googlers121913475
pharmgkbrs121913475
gwascentralrs121913475
openSNPrs121913475
23andMers121913475
23andMe allrs121913475
SNPshotrs121913475
SNPdbers121913475
MSV3drs121913475
GWAS Ctlgrs121913475
Max Magnitude0
ClinVar
Risk rs121913475(G;G)
Alt rs121913475(G;G)
Reference Rs121913475(A;A)
Significance Probable-Pathogenic
Disease Endometrial neoplasm
Variation info
Gene FGFR2
CLNDBN Endometrial neoplasm
Reversed 1
HGVS NC_000010.10:g.123279503T>C
CLNSRC
CLNACC RCV000438031.1,