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rs121909775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909775(C;T)
Make rs121909775(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position201205929
GeneCASP10
is asnp
is mentioned by
dbSNPrs121909775
ebirs121909775
HLIrs121909775
Exacrs121909775
Varsomers121909775
Maprs121909775
PheGenIrs121909775
hapmaprs121909775
1000 genomesrs121909775
hgdprs121909775
ensemblrs121909775
gopubmedrs121909775
geneviewrs121909775
scholarrs121909775
googlers121909775
pharmgkbrs121909775
gwascentralrs121909775
openSNPrs121909775
23andMers121909775
23andMe allrs121909775
SNP Nexus

SNPshotrs121909775
SNPdbers121909775
MSV3drs121909775
GWAS Ctlgrs121909775
Max Magnitude0
OMIM601762
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909775(A,T;A,T)
Alt rs121909775(A,T;A,T)
Reference rs121909775(C;C)
Significance Pathogenic
Disease Malignant lymphoma Neoplasm of stomach
Variation info
Gene CASP10
CLNDBN Malignant lymphoma, non-Hodgkin Neoplasm of stomach
Reversed 0
HGVS NC_000002.11:g.202070652C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008207.4, RCV000008208.4,