rs111033349

Orientation

minus

Stabilized

minus

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

Make rs111033349(A;A)

Make rs111033349(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

26461854

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033349
dbSNP (classic)	rs111033349
ClinGen	rs111033349
ebi	rs111033349
HLI	rs111033349
Exac	rs111033349
Gnomad	rs111033349
Varsome	rs111033349
LitVar	rs111033349
Map	rs111033349
PheGenI	rs111033349
Biobank	rs111033349
1000 genomes	rs111033349
hgdp	rs111033349
ensembl	rs111033349
geneview	rs111033349
scholar	rs111033349
google	rs111033349
pharmgkb	rs111033349
gwascentral	rs111033349
openSNP	rs111033349
23andMe	rs111033349
SNPshot	rs111033349
SNPdbe	rs111033349
MSV3d	rs111033349
GWAS Ctlg	rs111033349

Max Magnitude

0

ClinVar
Risk	rs111033349(A;A)
Alt	rs111033349(A;A)
Reference	Rs111033349(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness not provided
Variation	info
Gene	OTOF
CLNDBN	Nonsyndromic hearing loss and deafness not provided
Reversed	1
HGVS	NC_000002.11:g.26684722C>T
CLNSRC
CLNACC	RCV000041571.2, RCV000171287.1,