rs111033383

Orientation

minus

Stabilized

minus

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

Make rs111033383(A;A)

Make rs111033383(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26479325

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033383
dbSNP (classic)	rs111033383
ClinGen	rs111033383
ebi	rs111033383
HLI	rs111033383
Exac	rs111033383
Gnomad	rs111033383
Varsome	rs111033383
LitVar	rs111033383
Map	rs111033383
PheGenI	rs111033383
Biobank	rs111033383
1000 genomes	rs111033383
hgdp	rs111033383
ensembl	rs111033383
geneview	rs111033383
scholar	rs111033383
google	rs111033383
pharmgkb	rs111033383
gwascentral	rs111033383
openSNP	rs111033383
23andMe	rs111033383
SNPshot	rs111033383
SNPdbe	rs111033383
MSV3d	rs111033383
GWAS Ctlg	rs111033383

Max Magnitude

0

ClinVar
Risk	rs111033383(A;A)
Alt	rs111033383(A;A)
Reference	Rs111033383(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	OTOF
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000002.11:g.26702193C>T
CLNSRC	ClinVar
CLNACC	RCV000041483.2,