rs111033405

Orientation

minus

Stabilized

minus

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

Make rs111033405(C;C)

Make rs111033405(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26465753

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033405
dbSNP (classic)	rs111033405
ClinGen	rs111033405
ebi	rs111033405
HLI	rs111033405
Exac	rs111033405
Gnomad	rs111033405
Varsome	rs111033405
LitVar	rs111033405
Map	rs111033405
PheGenI	rs111033405
Biobank	rs111033405
1000 genomes	rs111033405
hgdp	rs111033405
ensembl	rs111033405
geneview	rs111033405
scholar	rs111033405
google	rs111033405
pharmgkb	rs111033405
gwascentral	rs111033405
openSNP	rs111033405
23andMe	rs111033405
SNPshot	rs111033405
SNPdbe	rs111033405
MSV3d	rs111033405
GWAS Ctlg	rs111033405

Max Magnitude

0

ClinVar
Risk	rs111033405(C;C)
Alt	rs111033405(C;C)
Reference	Rs111033405(T;T)
Significance	Other
Disease	Deafness Nonsyndromic hearing loss and deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9 Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000002.11:g.26688621A>G
CLNSRC	ClinVar
CLNACC	RCV000041550.4, RCV000211733.1,