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rs727503741

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503741(C;T)
Make rs727503741(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position74114349
GeneVCL
is asnp
is mentioned by
dbSNPrs727503741
ebirs727503741
HLIrs727503741
Exacrs727503741
Varsomers727503741
Maprs727503741
PheGenIrs727503741
hapmaprs727503741
1000 genomesrs727503741
hgdprs727503741
ensemblrs727503741
gopubmedrs727503741
geneviewrs727503741
scholarrs727503741
googlers727503741
pharmgkbrs727503741
gwascentralrs727503741
openSNPrs727503741
23andMers727503741
23andMe allrs727503741
SNP Nexus

SNPshotrs727503741
SNPdbers727503741
MSV3drs727503741
GWAS Ctlgrs727503741
Max Magnitude0
ClinVar
Risk rs727503741(T;T)
Alt rs727503741(T;T)
Reference rs727503741(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75874107C>T
CLNSRC
CLNACC RCV000152653.1,