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rs587779389

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779389(A;C)
Make rs587779389(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416890
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs587779389
ebirs587779389
HLIrs587779389
Exacrs587779389
Varsomers587779389
Maprs587779389
PheGenIrs587779389
hapmaprs587779389
1000 genomesrs587779389
hgdprs587779389
ensemblrs587779389
gopubmedrs587779389
geneviewrs587779389
scholarrs587779389
googlers587779389
pharmgkbrs587779389
gwascentralrs587779389
openSNPrs587779389
23andMers587779389
23andMe allrs587779389
SNP Nexus

SNPshotrs587779389
SNPdbers587779389
MSV3drs587779389
GWAS Ctlgrs587779389
Max Magnitude0
ClinVar
Risk rs587779389(C;C)
Alt rs587779389(C;C)
Reference rs587779389(A;A)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23886099T>G
CLNSRC
CLNACC RCV000132749.2,