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

rs786205603

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205603(C;T)
Make rs786205603(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position32438393
GeneDMD
is asnp
is mentioned by
dbSNPrs786205603
ebirs786205603
HLIrs786205603
Exacrs786205603
Varsomers786205603
Maprs786205603
PheGenIrs786205603
hapmaprs786205603
1000 genomesrs786205603
hgdprs786205603
ensemblrs786205603
gopubmedrs786205603
geneviewrs786205603
scholarrs786205603
googlers786205603
pharmgkbrs786205603
gwascentralrs786205603
openSNPrs786205603
23andMers786205603
23andMe allrs786205603
SNP Nexus

SNPshotrs786205603
SNPdbers786205603
MSV3drs786205603
GWAS Ctlgrs786205603
Max Magnitude0
ClinVar
Risk rs786205603(T;T)
Alt rs786205603(T;T)
Reference rs786205603(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32456510G>A
CLNSRC
CLNACC RCV000171432.1,