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rs587782961

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782961(A;G)
Make rs587782961(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23430936
GeneMYH7
is asnp
is mentioned by
dbSNPrs587782961
ClinGenrs587782961
ebirs587782961
HLIrs587782961
Exacrs587782961
Varsomers587782961
Maprs587782961
PheGenIrs587782961
hapmaprs587782961
1000 genomesrs587782961
hgdprs587782961
ensemblrs587782961
gopubmedrs587782961
geneviewrs587782961
scholarrs587782961
googlers587782961
pharmgkbrs587782961
gwascentralrs587782961
openSNPrs587782961
23andMers587782961
23andMe allrs587782961
SNP Nexus

SNPshotrs587782961
SNPdbers587782961
MSV3drs587782961
GWAS Ctlgrs587782961
Max Magnitude0
ClinVar
Risk rs587782961(G;G)
Alt rs587782961(G;G)
Reference Rs587782961(A;A)
Significance Probable-Pathogenic
Disease Left ventricular noncompaction cardiomyopathy
Variation info
Gene MYH7
CLNDBN Left ventricular noncompaction cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23900145T>C
CLNSRC
CLNACC RCV000143920.1,