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rs121909776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909776(C;C)
Make rs121909776(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position201187798
GeneCASP10
is asnp
is mentioned by
dbSNPrs121909776
ebirs121909776
HLIrs121909776
Exacrs121909776
Varsomers121909776
Maprs121909776
PheGenIrs121909776
hapmaprs121909776
1000 genomesrs121909776
hgdprs121909776
ensemblrs121909776
gopubmedrs121909776
geneviewrs121909776
scholarrs121909776
googlers121909776
pharmgkbrs121909776
gwascentralrs121909776
openSNPrs121909776
23andMers121909776
23andMe allrs121909776
SNP Nexus

SNPshotrs121909776
SNPdbers121909776
MSV3drs121909776
GWAS Ctlgrs121909776
GMAF0.0004591
Max Magnitude0
OMIM601762
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909776(C;C)
Alt rs121909776(C;C)
Reference rs121909776(T;T)
Significance Pathogenic
Disease Neoplasm of stomach
Variation info
Gene CASP10
CLNDBN Neoplasm of stomach
Reversed 0
HGVS NC_000002.11:g.202052521T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008210.4,