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rs398124049

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124049(-;-)
Make rs398124049(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31729739
GeneDMD
is asnp
is mentioned by
dbSNPrs398124049
ebirs398124049
HLIrs398124049
Exacrs398124049
Varsomers398124049
Maprs398124049
PheGenIrs398124049
hapmaprs398124049
1000 genomesrs398124049
hgdprs398124049
ensemblrs398124049
gopubmedrs398124049
geneviewrs398124049
scholarrs398124049
googlers398124049
pharmgkbrs398124049
gwascentralrs398124049
openSNPrs398124049
23andMers398124049
23andMe allrs398124049
SNP Nexus

SNPshotrs398124049
SNPdbers398124049
MSV3drs398124049
GWAS Ctlgrs398124049
Max Magnitude0
ClinVar
Risk rs398124049(;)
Alt rs398124049(;)
Reference rs398124049(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31747856delG
CLNSRC ClinVar
CLNACC RCV000080763.3,