rs398122848

Orientation

minus

Stabilized

minus

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

Make rs398122848(-;-)

Make rs398122848(-;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

21743752

Gene

SMPX

is a	snp
is	mentioned by
dbSNP	rs398122848
dbSNP (classic)	rs398122848
ClinGen	rs398122848
ebi	rs398122848
HLI	rs398122848
Exac	rs398122848
Gnomad	rs398122848
Varsome	rs398122848
LitVar	rs398122848
Map	rs398122848
PheGenI	rs398122848
Biobank	rs398122848
1000 genomes	rs398122848
hgdp	rs398122848
ensembl	rs398122848
geneview	rs398122848
scholar	rs398122848
google	rs398122848
pharmgkb	rs398122848
gwascentral	rs398122848
openSNP	rs398122848
23andMe	rs398122848
SNPshot	rs398122848
SNPdbe	rs398122848
MSV3d	rs398122848
GWAS Ctlg	rs398122848

Max Magnitude

0

ClinVar
Risk	rs398122848(-;-)
Alt	rs398122848(-;-)
Reference	Rs398122848(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	SMPX
CLNDBN	Deafness, X-linked 4
Reversed	1
HGVS	NC_000023.10:g.21761870delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022840.12,