rs267606975

Orientation

plus

Stabilized

plus

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

Make rs267606975(-;-)

Make rs267606975(-;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

83508975

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs267606975
dbSNP (classic)	rs267606975
ClinGen	rs267606975
ebi	rs267606975
HLI	rs267606975
Exac	rs267606975
Gnomad	rs267606975
Varsome	rs267606975
LitVar	rs267606975
Map	rs267606975
PheGenI	rs267606975
Biobank	rs267606975
1000 genomes	rs267606975
hgdp	rs267606975
ensembl	rs267606975
geneview	rs267606975
scholar	rs267606975
google	rs267606975
pharmgkb	rs267606975
gwascentral	rs267606975
openSNP	rs267606975
23andMe	rs267606975
SNPshot	rs267606975
SNPdbe	rs267606975
MSV3d	rs267606975
GWAS Ctlg	rs267606975

Max Magnitude

0

ClinVar
Risk	rs267606975(-;-)
Alt	rs267606975(-;-)
Reference	Rs267606975(G;G)
Significance	Untested
Disease	Deafness
Variation	info
Gene	POU3F4
CLNDBN	Deafness, X-linked 2
Reversed	0
HGVS	NC_000023.10:g.82763983delG
CLNSRC	ClinVar
CLNACC	RCV000144386.1,