rs111033373

Orientation

minus

Stabilized

minus

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

Make rs111033373(A;A)

Make rs111033373(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26462182

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033373
dbSNP (classic)	rs111033373
ClinGen	rs111033373
ebi	rs111033373
HLI	rs111033373
Exac	rs111033373
Gnomad	rs111033373
Varsome	rs111033373
LitVar	rs111033373
Map	rs111033373
PheGenI	rs111033373
Biobank	rs111033373
1000 genomes	rs111033373
hgdp	rs111033373
ensembl	rs111033373
geneview	rs111033373
scholar	rs111033373
google	rs111033373
pharmgkb	rs111033373
gwascentral	rs111033373
openSNP	rs111033373
23andMe	rs111033373
SNPshot	rs111033373
SNPdbe	rs111033373
MSV3d	rs111033373
GWAS Ctlg	rs111033373

Max Magnitude

0

ClinVar
Risk	rs111033373(A;A)
Alt	rs111033373(A;A)
Reference	Rs111033373(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness Deafness
Variation	info
Gene	OTOF
CLNDBN	Nonsyndromic hearing loss and deafness Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26685050C>T
CLNSRC	ClinVar
CLNACC	RCV000041568.2, RCV000225066.1,