rs128626236

Orientation

minus

Stabilized

minus

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

Make rs128626236(A;A)

Make rs128626236(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32816495

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs128626236
dbSNP (classic)	rs128626236
ClinGen	rs128626236
ebi	rs128626236
HLI	rs128626236
Exac	rs128626236
Gnomad	rs128626236
Varsome	rs128626236
LitVar	rs128626236
Map	rs128626236
PheGenI	rs128626236
Biobank	rs128626236
1000 genomes	rs128626236
hgdp	rs128626236
ensembl	rs128626236
geneview	rs128626236
scholar	rs128626236
google	rs128626236
pharmgkb	rs128626236
gwascentral	rs128626236
openSNP	rs128626236
23andMe	rs128626236
SNPshot	rs128626236
SNPdbe	rs128626236
MSV3d	rs128626236
GWAS Ctlg	rs128626236

Max Magnitude

0

OMIM	300377
Desc
Variant	0033
Related	also

ClinVar
Risk	rs128626236(A;A)
Alt	rs128626236(A;A)
Reference	Rs128626236(C;C)
Significance	Pathogenic
Disease	Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Becker muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32834612G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011981.17,