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

rs781036800

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs781036800(-;-)
Make rs781036800(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position74111991
GeneVCL
is asnp
is mentioned by
dbSNPrs781036800
ebirs781036800
HLIrs781036800
Exacrs781036800
Varsomers781036800
Maprs781036800
PheGenIrs781036800
hapmaprs781036800
1000 genomesrs781036800
hgdprs781036800
ensemblrs781036800
gopubmedrs781036800
geneviewrs781036800
scholarrs781036800
googlers781036800
pharmgkbrs781036800
gwascentralrs781036800
openSNPrs781036800
23andMers781036800
23andMe allrs781036800
SNP Nexus

SNPshotrs781036800
SNPdbers781036800
MSV3drs781036800
GWAS Ctlgrs781036800
Max Magnitude0
ClinVar
Risk rs781036800(;)
Alt rs781036800(;)
Reference rs781036800(CT;CT)
Significance Probable-Pathogenic
Disease not specified Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN not specified Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75871749_75871750delCT
CLNSRC
CLNACC RCV000184003.2, RCV000219138.1,