rs1060502630

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs1060502630(-;AA)

Make rs1060502630(AA;AA)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31169589

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502630
dbSNP (classic)	rs1060502630
ClinGen	rs1060502630
ebi	rs1060502630
HLI	rs1060502630
Exac	rs1060502630
Gnomad	rs1060502630
Varsome	rs1060502630
LitVar	rs1060502630
Map	rs1060502630
PheGenI	rs1060502630
Biobank	rs1060502630
1000 genomes	rs1060502630
hgdp	rs1060502630
ensembl	rs1060502630
geneview	rs1060502630
scholar	rs1060502630
google	rs1060502630
pharmgkb	rs1060502630
gwascentral	rs1060502630
openSNP	rs1060502630
23andMe	rs1060502630
SNPshot	rs1060502630
SNPdbe	rs1060502630
MSV3d	rs1060502630
GWAS Ctlg	rs1060502630

Max Magnitude

0

ClinVar
Risk	rs1060502630(AA;AA)
Alt	rs1060502630(AA;AA)
Reference	Rs1060502630(-;-)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31187706_31187707insTT
CLNSRC
CLNACC	RCV000475711.1,