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rs727503738

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503738(A;G)
Make rs727503738(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position74095654
GeneVCL
is asnp
is mentioned by
dbSNPrs727503738
ebirs727503738
HLIrs727503738
Exacrs727503738
Varsomers727503738
Maprs727503738
PheGenIrs727503738
hapmaprs727503738
1000 genomesrs727503738
hgdprs727503738
ensemblrs727503738
gopubmedrs727503738
geneviewrs727503738
scholarrs727503738
googlers727503738
pharmgkbrs727503738
gwascentralrs727503738
openSNPrs727503738
23andMers727503738
23andMe allrs727503738
SNP Nexus

SNPshotrs727503738
SNPdbers727503738
MSV3drs727503738
GWAS Ctlgrs727503738
Max Magnitude0
ClinVar
Risk rs727503738(G;G)
Alt rs727503738(G;G)
Reference rs727503738(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75855412A>G
CLNSRC
CLNACC RCV000152646.1,