Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs121913474

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913474(C;C)
Make rs121913474(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121515260
GeneFGFR2
is asnp
is mentioned by
dbSNPrs121913474
dbSNP (old)rs121913474
ClinGenrs121913474
ebirs121913474
HLIrs121913474
Exacrs121913474
Gnomadrs121913474
Varsomers121913474
Maprs121913474
PheGenIrs121913474
Biobankrs121913474
1000 genomesrs121913474
hgdprs121913474
ensemblrs121913474
gopubmedrs121913474
geneviewrs121913474
scholarrs121913474
googlers121913474
pharmgkbrs121913474
gwascentralrs121913474
openSNPrs121913474
23andMers121913474
23andMe allrs121913474
SNPshotrs121913474
SNPdbers121913474
MSV3drs121913474
GWAS Ctlgrs121913474
Max Magnitude0
ClinVar
Risk rs121913474(C;C)
Alt rs121913474(C;C)
Reference Rs121913474(T;T)
Significance Probable-Pathogenic
Disease Oesophageal carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach
Variation info
Gene FGFR2
CLNDBN Oesophageal carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach
Reversed 1
HGVS NC_000010.10:g.123274774A>G
CLNSRC
CLNACC RCV000419879.1, RCV000429923.1, RCV000440577.1,