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

rs121913476

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913476(A;A)
Make rs121913476(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121498520
GeneFGFR2
is asnp
is mentioned by
dbSNPrs121913476
dbSNP (old)rs121913476
ClinGenrs121913476
ebirs121913476
HLIrs121913476
Exacrs121913476
Gnomadrs121913476
Varsomers121913476
Maprs121913476
PheGenIrs121913476
Biobankrs121913476
1000 genomesrs121913476
hgdprs121913476
ensemblrs121913476
gopubmedrs121913476
geneviewrs121913476
scholarrs121913476
googlers121913476
pharmgkbrs121913476
gwascentralrs121913476
openSNPrs121913476
23andMers121913476
23andMe allrs121913476
SNPshotrs121913476
SNPdbers121913476
MSV3drs121913476
GWAS Ctlgrs121913476
Max Magnitude0
ClinVar
Risk rs121913476(A;A) rs121913476(G;G)
Alt rs121913476(A;A) rs121913476(G;G)
Reference Rs121913476(T;T)
Significance Probable-Pathogenic
Disease Endometrial Endometrioid Adenocarcinoma Adenocarcinoma of lung Nasopharyngeal Neoplasms Neoplasm of breast Malignant neoplasm of body of uterus
Variation info
Gene FGFR2
CLNDBN Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation Adenocarcinoma of lung Nasopharyngeal Neoplasms Neoplasm of breast Malignant neoplasm of body of uterus
Reversed 1
HGVS NC_000010.10:g.123258034A>C; NC_000010.10:g.123258034A>T
CLNSRC
CLNACC RCV000434110.1, RCV000424055.1, RCV000426965.1, RCV000433483.1, RCV000441770.1, RCV000443743.1,