rs111033455

Orientation

minus

Stabilized

minus

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

Make rs111033455(A;G)

Make rs111033455(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26460749

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033455
dbSNP (classic)	rs111033455
ClinGen	rs111033455
ebi	rs111033455
HLI	rs111033455
Exac	rs111033455
Gnomad	rs111033455
Varsome	rs111033455
LitVar	rs111033455
Map	rs111033455
PheGenI	rs111033455
Biobank	rs111033455
1000 genomes	rs111033455
hgdp	rs111033455
ensembl	rs111033455
geneview	rs111033455
scholar	rs111033455
google	rs111033455
pharmgkb	rs111033455
gwascentral	rs111033455
openSNP	rs111033455
23andMe	rs111033455
SNPshot	rs111033455
SNPdbe	rs111033455
MSV3d	rs111033455
GWAS Ctlg	rs111033455

Max Magnitude

0

ClinVar
Risk	rs111033455(G;G)
Alt	rs111033455(G;G)
Reference	Rs111033455(A;A)
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.26683617T>C
CLNSRC	ClinVar
CLNACC	RCV000041582.2,