Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520027

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520027(A;G)
Make rs1057520027(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121488005
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057520027
dbSNP (old)rs1057520027
ClinGenrs1057520027
ebirs1057520027
HLIrs1057520027
Exacrs1057520027
Gnomadrs1057520027
Varsomers1057520027
Maprs1057520027
PheGenIrs1057520027
Biobankrs1057520027
1000 genomesrs1057520027
hgdprs1057520027
ensemblrs1057520027
gopubmedrs1057520027
geneviewrs1057520027
scholarrs1057520027
googlers1057520027
pharmgkbrs1057520027
gwascentralrs1057520027
openSNPrs1057520027
23andMers1057520027
23andMe allrs1057520027
SNPshotrs1057520027
SNPdbers1057520027
MSV3drs1057520027
GWAS Ctlgrs1057520027
Max Magnitude0
ClinVar
Risk rs1057520027(G;G)
Alt rs1057520027(G;G)
Reference Rs1057520027(A;A)
Significance Probable-Pathogenic
Disease Endometrial neoplasm
Variation info
Gene FGFR2
CLNDBN Endometrial neoplasm
Reversed 1
HGVS NC_000010.10:g.123247519T>C
CLNSRC
CLNACC RCV000439319.1,