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rs1057519798

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519798(A;G)
Make rs1057519798(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121498528
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519798
dbSNP (old)rs1057519798
ClinGenrs1057519798
ebirs1057519798
HLIrs1057519798
Exacrs1057519798
Gnomadrs1057519798
Varsomers1057519798
Maprs1057519798
PheGenIrs1057519798
Biobankrs1057519798
1000 genomesrs1057519798
hgdprs1057519798
ensemblrs1057519798
gopubmedrs1057519798
geneviewrs1057519798
scholarrs1057519798
googlers1057519798
pharmgkbrs1057519798
gwascentralrs1057519798
openSNPrs1057519798
23andMers1057519798
23andMe allrs1057519798
SNPshotrs1057519798
SNPdbers1057519798
MSV3drs1057519798
GWAS Ctlgrs1057519798
Max Magnitude0
ClinVar
Risk rs1057519798(G;G)
Alt rs1057519798(G;G)
Reference Rs1057519798(A;A)
Significance Probable-Pathogenic
Disease Endometrial Endometrioid Adenocarcinoma
Variation info
Gene FGFR2
CLNDBN Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation
Reversed 1
HGVS NC_000010.10:g.123258042T>C
CLNSRC
CLNACC RCV000442792.1,