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rs794729010

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729010(G;T)
Make rs794729010(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154379795
GeneEMD
is asnp
is mentioned by
dbSNPrs794729010
ebirs794729010
HLIrs794729010
Exacrs794729010
Varsomers794729010
Maprs794729010
PheGenIrs794729010
hapmaprs794729010
1000 genomesrs794729010
hgdprs794729010
ensemblrs794729010
gopubmedrs794729010
geneviewrs794729010
scholarrs794729010
googlers794729010
pharmgkbrs794729010
gwascentralrs794729010
openSNPrs794729010
23andMers794729010
23andMe allrs794729010
SNP Nexus

SNPshotrs794729010
SNPdbers794729010
MSV3drs794729010
GWAS Ctlgrs794729010
Max Magnitude0
ClinVar
Risk rs794729010(T;T)
Alt rs794729010(T;T)
Reference rs794729010(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene EMD
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000023.10:g.153608155G>T
CLNSRC
CLNACC RCV000183441.1,