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rs1060502624

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACAA;ACAA) 0 common in clinvar
Make rs1060502624(-;-)
Make rs1060502624(-;ACAA)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31261000
GeneDMD
is asnp
is mentioned by
dbSNPrs1060502624
dbSNP (old)rs1060502624
ClinGenrs1060502624
ebirs1060502624
HLIrs1060502624
Exacrs1060502624
Gnomadrs1060502624
Varsomers1060502624
Maprs1060502624
PheGenIrs1060502624
Biobankrs1060502624
1000 genomesrs1060502624
hgdprs1060502624
ensemblrs1060502624
gopubmedrs1060502624
geneviewrs1060502624
scholarrs1060502624
googlers1060502624
pharmgkbrs1060502624
gwascentralrs1060502624
openSNPrs1060502624
23andMers1060502624
23andMe allrs1060502624
SNPshotrs1060502624
SNPdbers1060502624
MSV3drs1060502624
GWAS Ctlgrs1060502624
Max Magnitude0
ClinVar
Risk rs1060502624(-;-)
Alt rs1060502624(-;-)
Reference Rs1060502624(ACAA;ACAA)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31279117_31279120delTTGT
CLNSRC
CLNACC RCV000464817.1,