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rs797044602

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044602(C;C)
Make rs797044602(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23415669
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs797044602
ebirs797044602
HLIrs797044602
Exacrs797044602
Varsomers797044602
Maprs797044602
PheGenIrs797044602
hapmaprs797044602
1000 genomesrs797044602
hgdprs797044602
ensemblrs797044602
gopubmedrs797044602
geneviewrs797044602
scholarrs797044602
googlers797044602
pharmgkbrs797044602
gwascentralrs797044602
openSNPrs797044602
23andMers797044602
23andMe allrs797044602
SNP Nexus

SNPshotrs797044602
SNPdbers797044602
MSV3drs797044602
GWAS Ctlgrs797044602
Max Magnitude0
ClinVar
Risk rs797044602(C;C)
Alt rs797044602(C;C)
Reference rs797044602(T;T)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23884878A>G
CLNSRC
CLNACC RCV000192211.1,