rs111033446

Orientation

minus

Stabilized

minus

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

Make rs111033446(-;-)

Make rs111033446(-;AA)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26460988

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033446
dbSNP (classic)	rs111033446
ClinGen	rs111033446
ebi	rs111033446
HLI	rs111033446
Exac	rs111033446
Gnomad	rs111033446
Varsome	rs111033446
LitVar	rs111033446
Map	rs111033446
PheGenI	rs111033446
Biobank	rs111033446
1000 genomes	rs111033446
hgdp	rs111033446
ensembl	rs111033446
geneview	rs111033446
scholar	rs111033446
google	rs111033446
pharmgkb	rs111033446
gwascentral	rs111033446
openSNP	rs111033446
23andMe	rs111033446
SNPshot	rs111033446
SNPdbe	rs111033446
MSV3d	rs111033446
GWAS Ctlg	rs111033446

Max Magnitude

0

ClinVar
Risk	rs111033446(-;-)
Alt	rs111033446(-;-)
Reference	Rs111033446(AA;AA)
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.26683856_26683857delTT
CLNSRC	ClinVar
CLNACC	RCV000041577.2,