Have questions? Visit https://www.reddit.com/r/SNPedia

rs398124094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124094(A;A)
Make rs398124094(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31223046
GeneDMD
is asnp
is mentioned by
dbSNPrs398124094
ebirs398124094
HLIrs398124094
Exacrs398124094
Varsomers398124094
Maprs398124094
PheGenIrs398124094
hapmaprs398124094
1000 genomesrs398124094
hgdprs398124094
ensemblrs398124094
gopubmedrs398124094
geneviewrs398124094
scholarrs398124094
googlers398124094
pharmgkbrs398124094
gwascentralrs398124094
openSNPrs398124094
23andMers398124094
23andMe allrs398124094
SNP Nexus

SNPshotrs398124094
SNPdbers398124094
MSV3drs398124094
GWAS Ctlgrs398124094
Max Magnitude0
ClinVar
Risk rs398124094(A,C;A,C)
Alt rs398124094(A,C;A,C)
Reference rs398124094(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31241163C>G; NC_000023.10:g.31241163C>T
CLNSRC HGMD
CLNACC RCV000080840.4, RCV000179638.1, RCV000179639.1, RCV000080839.4, RCV000179642.1, RCV000179643.1,