rs111033384

Orientation

minus

Stabilized

minus

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

Make rs111033384(-;-)

Make rs111033384(-;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26460094

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033384
dbSNP (classic)	rs111033384
ClinGen	rs111033384
ebi	rs111033384
HLI	rs111033384
Exac	rs111033384
Gnomad	rs111033384
Varsome	rs111033384
LitVar	rs111033384
Map	rs111033384
PheGenI	rs111033384
Biobank	rs111033384
1000 genomes	rs111033384
hgdp	rs111033384
ensembl	rs111033384
geneview	rs111033384
scholar	rs111033384
google	rs111033384
pharmgkb	rs111033384
gwascentral	rs111033384
openSNP	rs111033384
23andMe	rs111033384
SNPshot	rs111033384
SNPdbe	rs111033384
MSV3d	rs111033384
GWAS Ctlg	rs111033384

Max Magnitude

0

ClinVar
Risk	rs111033384(-;-)
Alt	rs111033384(-;-)
Reference	Rs111033384(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	OTOF
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000002.11:g.26682962delC
CLNSRC
CLNACC	RCV000154421.1,