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rs587779396

From SNPedia

Orientationminus
Geno Mag Summary
(TGC;TGC) 0 common in clinvar
Make rs587779396(-;-)
Make rs587779396(-;TGC)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415174
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs587779396
ebirs587779396
HLIrs587779396
Exacrs587779396
Varsomers587779396
Maprs587779396
PheGenIrs587779396
hapmaprs587779396
1000 genomesrs587779396
hgdprs587779396
ensemblrs587779396
gopubmedrs587779396
geneviewrs587779396
scholarrs587779396
googlers587779396
pharmgkbrs587779396
gwascentralrs587779396
openSNPrs587779396
23andMers587779396
23andMe allrs587779396
SNP Nexus

SNPshotrs587779396
SNPdbers587779396
MSV3drs587779396
GWAS Ctlgrs587779396
Max Magnitude0
ClinVar
Risk rs587779396(;)
Alt rs587779396(;)
Reference rs587779396(TGC;TGC)
Significance Pathogenic
Disease Dilated cardiomyopathy 1S Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Dilated cardiomyopathy 1S Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23884383_23884385delGCA
CLNSRC
CLNACC RCV000132758.1, RCV000192203.1,