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rs587779415

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779415(C;C)
Make rs587779415(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416051
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs587779415
ebirs587779415
HLIrs587779415
Exacrs587779415
Varsomers587779415
Maprs587779415
PheGenIrs587779415
hapmaprs587779415
1000 genomesrs587779415
hgdprs587779415
ensemblrs587779415
gopubmedrs587779415
geneviewrs587779415
scholarrs587779415
googlers587779415
pharmgkbrs587779415
gwascentralrs587779415
openSNPrs587779415
23andMers587779415
23andMe allrs587779415
SNP Nexus

SNPshotrs587779415
SNPdbers587779415
MSV3drs587779415
GWAS Ctlgrs587779415
Max Magnitude0
ClinVar
Risk rs587779415(C;C)
Alt rs587779415(C;C)
Reference rs587779415(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23885260C>G
CLNSRC
CLNACC RCV000132761.2,