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rs1057520028

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520028(A;G)
Make rs1057520028(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121515283
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057520028
dbSNP (old)rs1057520028
ClinGenrs1057520028
ebirs1057520028
HLIrs1057520028
Exacrs1057520028
Gnomadrs1057520028
Varsomers1057520028
Maprs1057520028
PheGenIrs1057520028
Biobankrs1057520028
1000 genomesrs1057520028
hgdprs1057520028
ensemblrs1057520028
gopubmedrs1057520028
geneviewrs1057520028
scholarrs1057520028
googlers1057520028
pharmgkbrs1057520028
gwascentralrs1057520028
openSNPrs1057520028
23andMers1057520028
23andMe allrs1057520028
SNPshotrs1057520028
SNPdbers1057520028
MSV3drs1057520028
GWAS Ctlgrs1057520028
Max Magnitude0
ClinVar
Risk rs1057520028(G;G)
Alt rs1057520028(G;G)
Reference Rs1057520028(A;A)
Significance Probable-Pathogenic
Disease Endometrial neoplasm
Variation info
Gene FGFR2
CLNDBN Endometrial neoplasm
Reversed 1
HGVS NC_000010.10:g.123274797T>C
CLNSRC
CLNACC RCV000423432.1,