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rs727504381

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504381(C;T)
Make rs727504381(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position74097222
GeneVCL
is asnp
is mentioned by
dbSNPrs727504381
ebirs727504381
HLIrs727504381
Exacrs727504381
Varsomers727504381
Maprs727504381
PheGenIrs727504381
hapmaprs727504381
1000 genomesrs727504381
hgdprs727504381
ensemblrs727504381
gopubmedrs727504381
geneviewrs727504381
scholarrs727504381
googlers727504381
pharmgkbrs727504381
gwascentralrs727504381
openSNPrs727504381
23andMers727504381
23andMe allrs727504381
SNP Nexus

SNPshotrs727504381
SNPdbers727504381
MSV3drs727504381
GWAS Ctlgrs727504381
Max Magnitude0
ClinVar
Risk rs727504381(T;T)
Alt rs727504381(T;T)
Reference rs727504381(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75856980C>T
CLNSRC
CLNACC RCV000154540.1,