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

rs1057517960

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517960(A;A)
Make rs1057517960(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32595756
GeneDMD
is asnp
is mentioned by
dbSNPrs1057517960
dbSNP (classic)rs1057517960
ClinGenrs1057517960
ebirs1057517960
HLIrs1057517960
Exacrs1057517960
Gnomadrs1057517960
Varsomers1057517960
LitVarrs1057517960
Maprs1057517960
PheGenIrs1057517960
Biobankrs1057517960
1000 genomesrs1057517960
hgdprs1057517960
ensemblrs1057517960
geneviewrs1057517960
scholarrs1057517960
googlers1057517960
pharmgkbrs1057517960
gwascentralrs1057517960
openSNPrs1057517960
23andMers1057517960
23andMe allrs1057517960
SNPshotrs1057517960
SNPdbers1057517960
MSV3drs1057517960
GWAS Ctlgrs1057517960
Max Magnitude0
ClinVar
Risk rs1057517960(A;A)
Alt rs1057517960(A;A)
Reference Rs1057517960(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32613873C>T
CLNSRC
CLNACC RCV000413562.1,