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rs128627255

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs128627255(A;G)
Make rs128627255(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32697995
GeneDMD
is asnp
is mentioned by
dbSNPrs128627255
ClinGenrs128627255
ebirs128627255
HLIrs128627255
Exacrs128627255
Varsomers128627255
Maprs128627255
PheGenIrs128627255
Biobankrs128627255
1000 genomesrs128627255
hgdprs128627255
ensemblrs128627255
gopubmedrs128627255
geneviewrs128627255
scholarrs128627255
googlers128627255
pharmgkbrs128627255
gwascentralrs128627255
openSNPrs128627255
23andMers128627255
23andMe allrs128627255
SNP Nexus

SNPshotrs128627255
SNPdbers128627255
MSV3drs128627255
GWAS Ctlgrs128627255
Max Magnitude0
OMIM300377
Desc
Variant0073
Relatedalso
ClinVar
Risk rs128627255(G;G)
Alt rs128627255(G;G)
Reference Rs128627255(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32716112T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012030.17,