Have questions? Visit https://www.reddit.com/r/SNPedia

rs727505159

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727505159(C;T)
Make rs727505159(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position74114804
GeneVCL
is asnp
is mentioned by
dbSNPrs727505159
ebirs727505159
HLIrs727505159
Exacrs727505159
Varsomers727505159
Maprs727505159
PheGenIrs727505159
hapmaprs727505159
1000 genomesrs727505159
hgdprs727505159
ensemblrs727505159
gopubmedrs727505159
geneviewrs727505159
scholarrs727505159
googlers727505159
pharmgkbrs727505159
gwascentralrs727505159
openSNPrs727505159
23andMers727505159
23andMe allrs727505159
SNP Nexus

SNPshotrs727505159
SNPdbers727505159
MSV3drs727505159
GWAS Ctlgrs727505159
Max Magnitude0
ClinVar
Risk rs727505159(T;T)
Alt rs727505159(T;T)
Reference rs727505159(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75874562C>T
CLNSRC
CLNACC RCV000156630.1,