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rs121918314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918314(C;G)
Make rs121918314(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position85270792
GeneBCL10
is asnp
is mentioned by
dbSNPrs121918314
ebirs121918314
HLIrs121918314
Exacrs121918314
Varsomers121918314
Maprs121918314
PheGenIrs121918314
hapmaprs121918314
1000 genomesrs121918314
hgdprs121918314
ensemblrs121918314
gopubmedrs121918314
geneviewrs121918314
scholarrs121918314
googlers121918314
pharmgkbrs121918314
gwascentralrs121918314
openSNPrs121918314
23andMers121918314
23andMe allrs121918314
SNP Nexus

SNPshotrs121918314
SNPdbers121918314
MSV3drs121918314
GWAS Ctlgrs121918314
Max Magnitude0
OMIM603517
Desc
Variant0016
Relatedalso
OMIM603517
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121918314(G,T;G,T)
Alt rs121918314(G,T;G,T)
Reference rs121918314(C;C)
Significance Pathogenic
Disease Male germ cell tumor
Variation info
Gene BCL10
CLNDBN Male germ cell tumor, somatic
Reversed 1
HGVS NC_000001.10:g.85736475G>A; NC_000001.10:g.85736475G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006644.4, RCV000006643.4,