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rs1057519800

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519800(G;T)
Make rs1057519800(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121498562
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519800
dbSNP (classic)rs1057519800
ClinGenrs1057519800
ebirs1057519800
HLIrs1057519800
Exacrs1057519800
Gnomadrs1057519800
Varsomers1057519800
LitVarrs1057519800
Maprs1057519800
PheGenIrs1057519800
Biobankrs1057519800
1000 genomesrs1057519800
hgdprs1057519800
ensemblrs1057519800
geneviewrs1057519800
scholarrs1057519800
googlers1057519800
pharmgkbrs1057519800
gwascentralrs1057519800
openSNPrs1057519800
23andMers1057519800
23andMe allrs1057519800
SNPshotrs1057519800
SNPdbers1057519800
MSV3drs1057519800
GWAS Ctlgrs1057519800
Max Magnitude0
ClinVar
Risk rs1057519800(A;A) rs1057519800(C;C) rs1057519800(T;T)
Alt rs1057519800(A;A) rs1057519800(C;C) rs1057519800(T;T)
Reference Rs1057519800(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.123258076C>A; NC_000010.10:g.123258076C>G; NC_000010.10:g.123258076C>T
CLNSRC
CLNACC RCV000424365.1, RCV000435530.1, RCV000417871.1,