rs111033447

Orientation

minus

Stabilized

minus

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

Make rs111033447(A;A)

Make rs111033447(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26495011

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033447
dbSNP (classic)	rs111033447
ClinGen	rs111033447
ebi	rs111033447
HLI	rs111033447
Exac	rs111033447
Gnomad	rs111033447
Varsome	rs111033447
LitVar	rs111033447
Map	rs111033447
PheGenI	rs111033447
Biobank	rs111033447
1000 genomes	rs111033447
hgdp	rs111033447
ensembl	rs111033447
geneview	rs111033447
scholar	rs111033447
google	rs111033447
pharmgkb	rs111033447
gwascentral	rs111033447
openSNP	rs111033447
23andMe	rs111033447
SNPshot	rs111033447
SNPdbe	rs111033447
MSV3d	rs111033447
GWAS Ctlg	rs111033447

Max Magnitude

0

ClinVar
Risk	rs111033447(A;A) rs111033447(T;T)
Alt	rs111033447(A;A) rs111033447(T;T)
Reference	Rs111033447(C;C)
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.26717879G>T
CLNSRC	ClinVar
CLNACC	RCV000041590.2,