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rs1057519900

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519900(A;A)
Make rs1057519900(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121515259
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519900
dbSNP (old)rs1057519900
ClinGenrs1057519900
ebirs1057519900
HLIrs1057519900
Exacrs1057519900
Gnomadrs1057519900
Varsomers1057519900
Maprs1057519900
PheGenIrs1057519900
Biobankrs1057519900
1000 genomesrs1057519900
hgdprs1057519900
ensemblrs1057519900
gopubmedrs1057519900
geneviewrs1057519900
scholarrs1057519900
googlers1057519900
pharmgkbrs1057519900
gwascentralrs1057519900
openSNPrs1057519900
23andMers1057519900
23andMe allrs1057519900
SNPshotrs1057519900
SNPdbers1057519900
MSV3drs1057519900
GWAS Ctlgrs1057519900
Max Magnitude0
ClinVar
Risk rs1057519900(A;A)
Alt rs1057519900(A;A)
Reference Rs1057519900(G;G)
Significance Probable-Pathogenic
Disease Oesophageal carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach
Variation info
Gene FGFR2
CLNDBN Oesophageal carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach
Reversed 1
HGVS NC_000010.10:g.123274773C>T
CLNSRC
CLNACC RCV000421261.1, RCV000434751.1, RCV000438442.1,