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rs71579353

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs71579353(A;A)
Make rs71579353(A;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position74082499
GeneVCL
is asnp
is mentioned by
dbSNPrs71579353
ebirs71579353
HLIrs71579353
Exacrs71579353
Varsomers71579353
Maprs71579353
PheGenIrs71579353
hapmaprs71579353
1000 genomesrs71579353
hgdprs71579353
ensemblrs71579353
gopubmedrs71579353
geneviewrs71579353
scholarrs71579353
googlers71579353
pharmgkbrs71579353
gwascentralrs71579353
openSNPrs71579353
23andMers71579353
23andMe allrs71579353
SNP Nexus

SNPshotrs71579353
SNPdbers71579353
MSV3drs71579353
GWAS Ctlgrs71579353
Max Magnitude0
OMIM193065
Desc
Variant0003
Relatedalso


ClinVar
Risk rs71579353(A;A)
Alt rs71579353(A;A)
Reference rs71579353(C;C)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 15
Variation info
Gene VCL
CLNDBN Familial hypertrophic cardiomyopathy 15
Reversed 0
HGVS NC_000010.10:g.75842257C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012982.16,