rs111033345

Orientation

plus

Stabilized

plus

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

Make rs111033345(C;T)

Make rs111033345(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

83508823

Gene

POU3F4

is a	snp
is	mentioned by
dbSNP	rs111033345
dbSNP (classic)	rs111033345
ClinGen	rs111033345
ebi	rs111033345
HLI	rs111033345
Exac	rs111033345
Gnomad	rs111033345
Varsome	rs111033345
LitVar	rs111033345
Map	rs111033345
PheGenI	rs111033345
Biobank	rs111033345
1000 genomes	rs111033345
hgdp	rs111033345
ensembl	rs111033345
geneview	rs111033345
scholar	rs111033345
google	rs111033345
pharmgkb	rs111033345
gwascentral	rs111033345
openSNP	rs111033345
23andMe	rs111033345
SNPshot	rs111033345
SNPdbe	rs111033345
MSV3d	rs111033345
GWAS Ctlg	rs111033345

Max Magnitude

0

ClinVar
Risk	rs111033345(T;T)
Alt	rs111033345(T;T)
Reference	Rs111033345(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	POU3F4
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000023.10:g.82763831C>T
CLNSRC	ClinVar
CLNACC	RCV000036255.2,