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rs1057519796

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519796(A;A)
Make rs1057519796(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121496546
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519796
dbSNP (old)rs1057519796
ClinGenrs1057519796
ebirs1057519796
HLIrs1057519796
Exacrs1057519796
Gnomadrs1057519796
Varsomers1057519796
Maprs1057519796
PheGenIrs1057519796
Biobankrs1057519796
1000 genomesrs1057519796
hgdprs1057519796
ensemblrs1057519796
gopubmedrs1057519796
geneviewrs1057519796
scholarrs1057519796
googlers1057519796
pharmgkbrs1057519796
gwascentralrs1057519796
openSNPrs1057519796
23andMers1057519796
23andMe allrs1057519796
SNPshotrs1057519796
SNPdbers1057519796
MSV3drs1057519796
GWAS Ctlgrs1057519796
Max Magnitude0
ClinVar
Risk rs1057519796(A;A)
Alt rs1057519796(A;A)
Reference Rs1057519796(T;T)
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.123256060A>T
CLNSRC
CLNACC RCV000428728.1,