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rs1057519799

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519799(G;T)
Make rs1057519799(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121498556
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519799
dbSNP (old)rs1057519799
ClinGenrs1057519799
ebirs1057519799
HLIrs1057519799
Exacrs1057519799
Gnomadrs1057519799
Varsomers1057519799
Maprs1057519799
PheGenIrs1057519799
Biobankrs1057519799
1000 genomesrs1057519799
hgdprs1057519799
ensemblrs1057519799
gopubmedrs1057519799
geneviewrs1057519799
scholarrs1057519799
googlers1057519799
pharmgkbrs1057519799
gwascentralrs1057519799
openSNPrs1057519799
23andMers1057519799
23andMe allrs1057519799
SNPshotrs1057519799
SNPdbers1057519799
MSV3drs1057519799
GWAS Ctlgrs1057519799
Max Magnitude0
ClinVar
Risk rs1057519799(A;A) rs1057519799(C;C) rs1057519799(T;T)
Alt rs1057519799(A;A) rs1057519799(C;C) rs1057519799(T;T)
Reference Rs1057519799(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.123258070C>A; NC_000010.10:g.123258070C>G; NC_000010.10:g.123258070C>T
CLNSRC
CLNACC RCV000425939.1, RCV000436200.1, RCV000442661.1,