rs111033342

Orientation

minus

Stabilized

minus

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

Make rs111033342(A;A)

Make rs111033342(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26467234

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033342
dbSNP (classic)	rs111033342
ClinGen	rs111033342
ebi	rs111033342
HLI	rs111033342
Exac	rs111033342
Gnomad	rs111033342
Varsome	rs111033342
LitVar	rs111033342
Map	rs111033342
PheGenI	rs111033342
Biobank	rs111033342
1000 genomes	rs111033342
hgdp	rs111033342
ensembl	rs111033342
geneview	rs111033342
scholar	rs111033342
google	rs111033342
pharmgkb	rs111033342
gwascentral	rs111033342
openSNP	rs111033342
23andMe	rs111033342
SNPshot	rs111033342
SNPdbe	rs111033342
MSV3d	rs111033342
GWAS Ctlg	rs111033342

Max Magnitude

0

ClinVar
Risk	rs111033342(A;A) rs111033342(T;T)
Alt	rs111033342(A;A) rs111033342(T;T)
Reference	Rs111033342(G;G)
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.26690102C>T
CLNSRC	ClinVar
CLNACC	RCV000041540.2,