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rs587779414

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779414(C;C)
Make rs587779414(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417230
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs587779414
ebirs587779414
HLIrs587779414
Exacrs587779414
Varsomers587779414
Maprs587779414
PheGenIrs587779414
hapmaprs587779414
1000 genomesrs587779414
hgdprs587779414
ensemblrs587779414
gopubmedrs587779414
geneviewrs587779414
scholarrs587779414
googlers587779414
pharmgkbrs587779414
gwascentralrs587779414
openSNPrs587779414
23andMers587779414
23andMe allrs587779414
SNP Nexus

SNPshotrs587779414
SNPdbers587779414
MSV3drs587779414
GWAS Ctlgrs587779414
Max Magnitude0
ClinVar
Risk rs587779414(C;C)
Alt rs587779414(C;C)
Reference rs587779414(T;T)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23886439A>G
CLNSRC
CLNACC RCV000132747.2,