Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779390

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779390(A;C)
Make rs587779390(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416162
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs587779390
ebirs587779390
HLIrs587779390
Exacrs587779390
Varsomers587779390
Maprs587779390
PheGenIrs587779390
hapmaprs587779390
1000 genomesrs587779390
hgdprs587779390
ensemblrs587779390
gopubmedrs587779390
geneviewrs587779390
scholarrs587779390
googlers587779390
pharmgkbrs587779390
gwascentralrs587779390
openSNPrs587779390
23andMers587779390
23andMe allrs587779390
SNP Nexus

SNPshotrs587779390
SNPdbers587779390
MSV3drs587779390
GWAS Ctlgrs587779390
Max Magnitude0
ClinVar
Risk rs587779390(C;C)
Alt rs587779390(C;C)
Reference rs587779390(A;A)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23885371T>G
CLNSRC
CLNACC RCV000132750.2,