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rs797044598

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044598(A;A)
Make rs797044598(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23414096
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs797044598
ebirs797044598
HLIrs797044598
Exacrs797044598
Varsomers797044598
Maprs797044598
PheGenIrs797044598
hapmaprs797044598
1000 genomesrs797044598
hgdprs797044598
ensemblrs797044598
gopubmedrs797044598
geneviewrs797044598
scholarrs797044598
googlers797044598
pharmgkbrs797044598
gwascentralrs797044598
openSNPrs797044598
23andMers797044598
23andMe allrs797044598
SNP Nexus

SNPshotrs797044598
SNPdbers797044598
MSV3drs797044598
GWAS Ctlgrs797044598
Max Magnitude0
ClinVar
Risk rs797044598(A;A)
Alt rs797044598(A;A)
Reference rs797044598(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23883305C>T
CLNSRC
CLNACC RCV000192204.1,