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rs1057519797

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519797(A;A)
Make rs1057519797(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121496705
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519797
dbSNP (old)rs1057519797
ClinGenrs1057519797
ebirs1057519797
HLIrs1057519797
Exacrs1057519797
Gnomadrs1057519797
Varsomers1057519797
Maprs1057519797
PheGenIrs1057519797
Biobankrs1057519797
1000 genomesrs1057519797
hgdprs1057519797
ensemblrs1057519797
gopubmedrs1057519797
geneviewrs1057519797
scholarrs1057519797
googlers1057519797
pharmgkbrs1057519797
gwascentralrs1057519797
openSNPrs1057519797
23andMers1057519797
23andMe allrs1057519797
SNPshotrs1057519797
SNPdbers1057519797
MSV3drs1057519797
GWAS Ctlgrs1057519797
Max Magnitude0
ClinVar
Risk rs1057519797(A;A)
Alt rs1057519797(A;A)
Reference Rs1057519797(G;G)
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.123256219C>T
CLNSRC
CLNACC RCV000423825.1,