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rs1057520029

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520029(A;T)
Make rs1057520029(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121488003
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057520029
dbSNP (old)rs1057520029
ClinGenrs1057520029
ebirs1057520029
HLIrs1057520029
Exacrs1057520029
Gnomadrs1057520029
Varsomers1057520029
LitVarrs1057520029
Maprs1057520029
PheGenIrs1057520029
Biobankrs1057520029
1000 genomesrs1057520029
hgdprs1057520029
ensemblrs1057520029
gopubmedrs1057520029
geneviewrs1057520029
scholarrs1057520029
googlers1057520029
pharmgkbrs1057520029
gwascentralrs1057520029
openSNPrs1057520029
23andMers1057520029
23andMe allrs1057520029
SNPshotrs1057520029
SNPdbers1057520029
MSV3drs1057520029
GWAS Ctlgrs1057520029
Max Magnitude0
ClinVar
Risk rs1057520029(T;T)
Alt rs1057520029(T;T)
Reference Rs1057520029(A;A)
Significance Probable-Pathogenic
Disease Endometrial neoplasm
Variation info
Gene FGFR2
CLNDBN Endometrial neoplasm
Reversed 1
HGVS NC_000010.10:g.123247517T>A
CLNSRC
CLNACC RCV000433692.1,