rs387906707

Orientation

minus

Stabilized

minus

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

Make rs387906707(G;T)

Make rs387906707(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

21743773

Gene

SMPX

is a	snp
is	mentioned by
dbSNP	rs387906707
dbSNP (classic)	rs387906707
ClinGen	rs387906707
ebi	rs387906707
HLI	rs387906707
Exac	rs387906707
Gnomad	rs387906707
Varsome	rs387906707
LitVar	rs387906707
Map	rs387906707
PheGenI	rs387906707
Biobank	rs387906707
1000 genomes	rs387906707
hgdp	rs387906707
ensembl	rs387906707
geneview	rs387906707
scholar	rs387906707
google	rs387906707
pharmgkb	rs387906707
gwascentral	rs387906707
openSNP	rs387906707
23andMe	rs387906707
SNPshot	rs387906707
SNPdbe	rs387906707
MSV3d	rs387906707
GWAS Ctlg	rs387906707

Max Magnitude

0

ClinVar
Risk	rs387906707(T;T)
Alt	rs387906707(T;T)
Reference	Rs387906707(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	SMPX
CLNDBN	Deafness, X-linked 4
Reversed	1
HGVS	NC_000023.10:g.21761891C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022838.11,