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

rs121913652

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913652(A;A)
Make rs121913652(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23414015
GeneMYH7
is asnp
is mentioned by
dbSNPrs121913652
ebirs121913652
HLIrs121913652
Exacrs121913652
Varsomers121913652
Maprs121913652
PheGenIrs121913652
hapmaprs121913652
1000 genomesrs121913652
hgdprs121913652
ensemblrs121913652
gopubmedrs121913652
geneviewrs121913652
scholarrs121913652
googlers121913652
pharmgkbrs121913652
gwascentralrs121913652
openSNPrs121913652
23andMers121913652
23andMe allrs121913652
SNP Nexus

SNPshotrs121913652
SNPdbers121913652
MSV3drs121913652
GWAS Ctlgrs121913652
Max Magnitude0
OMIM160760
Desc
Variant0035
Relatedalso
ClinVar
Risk rs121913652(A;A)
Alt rs121913652(A;A)
Reference rs121913652(G;G)
Significance Pathogenic
Disease Myopathy not specified
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, myosin storage, autosomal recessive not specified
Reversed 1
HGVS NC_000014.8:g.23883224C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015178.26, RCV000156689.2,