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rs147546024

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs147546024(A;G)
Make rs147546024(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position33127969
GeneDMD
is asnp
is mentioned by
dbSNPrs147546024
ebirs147546024
HLIrs147546024
Exacrs147546024
Varsomers147546024
Maprs147546024
PheGenIrs147546024
hapmaprs147546024
1000 genomesrs147546024
hgdprs147546024
ensemblrs147546024
gopubmedrs147546024
geneviewrs147546024
scholarrs147546024
googlers147546024
pharmgkbrs147546024
gwascentralrs147546024
openSNPrs147546024
23andMers147546024
23andMe allrs147546024
SNP Nexus

SNPshotrs147546024
SNPdbers147546024
MSV3drs147546024
GWAS Ctlgrs147546024
Max Magnitude0

[PMID 25227141] The dystrophin gene and cognitive function in the general population

ClinVar
Risk rs147546024(G;G)
Alt rs147546024(G;G)
Reference rs147546024(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene DMD
CLNDBN not specified
Reversed 0
HGVS NC_000023.10:g.33146086A>G
CLNSRC ClinVar
CLNACC RCV000080561.3,