rs730882189

Orientation

plus

Stabilized

plus

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

Make rs730882189(-;-)

Make rs730882189(-;AGTG)

Make rs730882189(AGTG;AGTG)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

83509186

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs730882189
dbSNP (classic)	rs730882189
ClinGen	rs730882189
ebi	rs730882189
HLI	rs730882189
Exac	rs730882189
Gnomad	rs730882189
Varsome	rs730882189
LitVar	rs730882189
Map	rs730882189
PheGenI	rs730882189
Biobank	rs730882189
1000 genomes	rs730882189
hgdp	rs730882189
ensembl	rs730882189
geneview	rs730882189
scholar	rs730882189
google	rs730882189
pharmgkb	rs730882189
gwascentral	rs730882189
openSNP	rs730882189
23andMe	rs730882189
SNPshot	rs730882189
SNPdbe	rs730882189
MSV3d	rs730882189
GWAS Ctlg	rs730882189

Max Magnitude

0

ClinVar
Risk	rs730882189(-;-)
Alt	rs730882189(-;-)
Reference	Rs730882189(GTGA;GTGA)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	POU3F4
CLNDBN	Deafness, X-linked 2
Reversed	0
HGVS	NC_000023.10:g.82764194_82764197delAGTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012447.23,