rs387906708

Orientation

minus

Stabilized

minus

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

Make rs387906708(G;T)

Make rs387906708(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

21737616

Gene

SMPX

is a	snp
is	mentioned by
dbSNP	rs387906708
dbSNP (classic)	rs387906708
ClinGen	rs387906708
ebi	rs387906708
HLI	rs387906708
Exac	rs387906708
Gnomad	rs387906708
Varsome	rs387906708
LitVar	rs387906708
Map	rs387906708
PheGenI	rs387906708
Biobank	rs387906708
1000 genomes	rs387906708
hgdp	rs387906708
ensembl	rs387906708
geneview	rs387906708
scholar	rs387906708
google	rs387906708
pharmgkb	rs387906708
gwascentral	rs387906708
openSNP	rs387906708
23andMe	rs387906708
SNPshot	rs387906708
SNPdbe	rs387906708
MSV3d	rs387906708
GWAS Ctlg	rs387906708

Max Magnitude

0

ClinVar
Risk	rs387906708(T;T)
Alt	rs387906708(T;T)
Reference	Rs387906708(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	SMPX
CLNDBN	Deafness, X-linked 4
Reversed	1
HGVS	NC_000023.10:g.21755734C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022839.21,