rs1060499590

Orientation

minus

Stabilized

minus

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

Make rs1060499590(A;A)

Make rs1060499590(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

21737698

Gene

SMPX

is a	snp
is	mentioned by
dbSNP	rs1060499590
dbSNP (classic)	rs1060499590
ClinGen	rs1060499590
ebi	rs1060499590
HLI	rs1060499590
Exac	rs1060499590
Gnomad	rs1060499590
Varsome	rs1060499590
LitVar	rs1060499590
Map	rs1060499590
PheGenI	rs1060499590
Biobank	rs1060499590
1000 genomes	rs1060499590
hgdp	rs1060499590
ensembl	rs1060499590
geneview	rs1060499590
scholar	rs1060499590
google	rs1060499590
pharmgkb	rs1060499590
gwascentral	rs1060499590
openSNP	rs1060499590
23andMe	rs1060499590
SNPshot	rs1060499590
SNPdbe	rs1060499590
MSV3d	rs1060499590
GWAS Ctlg	rs1060499590

Max Magnitude

0

ClinVar
Risk	rs1060499590(A;A)
Alt	rs1060499590(A;A)
Reference	Rs1060499590(G;G)
Significance	Probable-Pathogenic
Disease	Deafness
Variation	info
Gene	SMPX
CLNDBN	Deafness, X-linked 4
Reversed	1
HGVS	NC_000023.10:g.21755816C>T
CLNSRC
CLNACC	RCV000477909.1,