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rs121917776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917776(C;T)
Make rs121917776(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position74112086
GeneVCL
is asnp
is mentioned by
dbSNPrs121917776
ebirs121917776
HLIrs121917776
Exacrs121917776
Varsomers121917776
Maprs121917776
PheGenIrs121917776
hapmaprs121917776
1000 genomesrs121917776
hgdprs121917776
ensemblrs121917776
gopubmedrs121917776
geneviewrs121917776
scholarrs121917776
googlers121917776
pharmgkbrs121917776
gwascentralrs121917776
openSNPrs121917776
23andMers121917776
23andMe allrs121917776
SNP Nexus

SNPshotrs121917776
SNPdbers121917776
MSV3drs121917776
GWAS Ctlgrs121917776
Max Magnitude0
OMIM193065
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121917776(T;T)
Alt rs121917776(T;T)
Reference rs121917776(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1W Familial hypertrophic cardiomyopathy 15
Variation info
Gene VCL
CLNDBN Dilated cardiomyopathy 1W Familial hypertrophic cardiomyopathy 15
Reversed 0
HGVS NC_000010.10:g.75871844C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012980.16, RCV000012981.22,