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rs587782962

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782962(A;A)
Make rs587782962(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23422267
GeneMYH7
is asnp
is mentioned by
dbSNPrs587782962
ebirs587782962
HLIrs587782962
Exacrs587782962
Varsomers587782962
Maprs587782962
PheGenIrs587782962
hapmaprs587782962
1000 genomesrs587782962
hgdprs587782962
ensemblrs587782962
gopubmedrs587782962
geneviewrs587782962
scholarrs587782962
googlers587782962
pharmgkbrs587782962
gwascentralrs587782962
openSNPrs587782962
23andMers587782962
23andMe allrs587782962
SNP Nexus

SNPshotrs587782962
SNPdbers587782962
MSV3drs587782962
GWAS Ctlgrs587782962
Max Magnitude0
ClinVar
Risk rs587782962(A;A)
Alt rs587782962(A;A)
Reference rs587782962(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23891476C>T
CLNSRC
CLNACC RCV000143923.4, RCV000158590.2,