rs186810296

Orientation

plus

Stabilized

plus

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

Make rs186810296(C;T)

Make rs186810296(T;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

26470592

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs186810296
dbSNP (classic)	rs186810296
ClinGen	rs186810296
ebi	rs186810296
HLI	rs186810296
Exac	rs186810296
Gnomad	rs186810296
Varsome	rs186810296
LitVar	rs186810296
Map	rs186810296
PheGenI	rs186810296
Biobank	rs186810296
1000 genomes	rs186810296
hgdp	rs186810296
ensembl	rs186810296
geneview	rs186810296
scholar	rs186810296
google	rs186810296
pharmgkb	rs186810296
gwascentral	rs186810296
openSNP	rs186810296
23andMe	rs186810296
SNPshot	rs186810296
SNPdbe	rs186810296
MSV3d	rs186810296
GWAS Ctlg	rs186810296

Max Magnitude

0

ClinVar
Risk	rs186810296(T;T)
Alt	rs186810296(T;T)
Reference	Rs186810296(C;C)
Significance	Pathogenic
Disease	not specified Deafness
Variation	info
Gene	OTOF
CLNDBN	not specified Deafness, autosomal recessive 9
Reversed	0
HGVS	NC_000002.11:g.26693460C>T
CLNSRC	ClinVar
CLNACC	RCV000041538.3, RCV000490336.1,