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rs797044601

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044601(C;C)
Make rs797044601(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23415799
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs797044601
ebirs797044601
HLIrs797044601
Exacrs797044601
Varsomers797044601
Maprs797044601
PheGenIrs797044601
hapmaprs797044601
1000 genomesrs797044601
hgdprs797044601
ensemblrs797044601
gopubmedrs797044601
geneviewrs797044601
scholarrs797044601
googlers797044601
pharmgkbrs797044601
gwascentralrs797044601
openSNPrs797044601
23andMers797044601
23andMe allrs797044601
SNP Nexus

SNPshotrs797044601
SNPdbers797044601
MSV3drs797044601
GWAS Ctlgrs797044601
Max Magnitude0
ClinVar
Risk rs797044601(C;C)
Alt rs797044601(C;C)
Reference rs797044601(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23885008C>G
CLNSRC
CLNACC RCV000192210.1,