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rs370644567

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs370644567(A;G)
Make rs370644567(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32573618
GeneDMD
is asnp
is mentioned by
dbSNPrs370644567
ebirs370644567
HLIrs370644567
Exacrs370644567
Varsomers370644567
Maprs370644567
PheGenIrs370644567
hapmaprs370644567
1000 genomesrs370644567
hgdprs370644567
ensemblrs370644567
gopubmedrs370644567
geneviewrs370644567
scholarrs370644567
googlers370644567
pharmgkbrs370644567
gwascentralrs370644567
openSNPrs370644567
23andMers370644567
23andMe allrs370644567
SNP Nexus

SNPshotrs370644567
SNPdbers370644567
MSV3drs370644567
GWAS Ctlgrs370644567
Max Magnitude0
ClinVar
Risk rs370644567(G;G)
Alt rs370644567(G;G)
Reference rs370644567(A;A)
Significance Pathogenic
Disease Exertional myalgia Becker muscular dystrophy not specified
Variation info
Gene DMD
CLNDBN Exertional myalgia, muscle stiffness and myoglobinuria Becker muscular dystrophy not specified
Reversed 0
HGVS NC_000023.10:g.32591735A>G
CLNSRC
CLNACC RCV000148464.1, RCV000174887.1, RCV000223816.2,