rs111033343

Orientation

plus

Stabilized

plus

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

Make rs111033343(A;A)

Make rs111033343(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

83508665

Gene	LOC107985635, POU3F4

is a	snp
is	mentioned by
dbSNP	rs111033343
dbSNP (classic)	rs111033343
ClinGen	rs111033343
ebi	rs111033343
HLI	rs111033343
Exac	rs111033343
Gnomad	rs111033343
Varsome	rs111033343
LitVar	rs111033343
Map	rs111033343
PheGenI	rs111033343
Biobank	rs111033343
1000 genomes	rs111033343
hgdp	rs111033343
ensembl	rs111033343
geneview	rs111033343
scholar	rs111033343
google	rs111033343
pharmgkb	rs111033343
gwascentral	rs111033343
openSNP	rs111033343
23andMe	rs111033343
SNPshot	rs111033343
SNPdbe	rs111033343
MSV3d	rs111033343
GWAS Ctlg	rs111033343

Max Magnitude

0

ClinVar
Risk	rs111033343(A;A)
Alt	rs111033343(A;A)
Reference	Rs111033343(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	POU3F4
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000023.10:g.82763673G>A
CLNSRC	ClinVar
CLNACC	RCV000036254.2,