rs387906706

Orientation

minus

Stabilized

minus

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

Make rs387906706(G;T)

Make rs387906706(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

21737655

Gene

SMPX

is a	snp
is	mentioned by
dbSNP	rs387906706
dbSNP (classic)	rs387906706
ClinGen	rs387906706
ebi	rs387906706
HLI	rs387906706
Exac	rs387906706
Gnomad	rs387906706
Varsome	rs387906706
LitVar	rs387906706
Map	rs387906706
PheGenI	rs387906706
Biobank	rs387906706
1000 genomes	rs387906706
hgdp	rs387906706
ensembl	rs387906706
geneview	rs387906706
scholar	rs387906706
google	rs387906706
pharmgkb	rs387906706
gwascentral	rs387906706
openSNP	rs387906706
23andMe	rs387906706
SNPshot	rs387906706
SNPdbe	rs387906706
MSV3d	rs387906706
GWAS Ctlg	rs387906706

Max Magnitude

0

ClinVar
Risk	rs387906706(T;T)
Alt	rs387906706(T;T)
Reference	Rs387906706(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	SMPX
CLNDBN	Deafness, X-linked 4
Reversed	1
HGVS	NC_000023.10:g.21755773C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022837.24,