rs111033370

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype

Make rs111033370(-;A)

Make rs111033370(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26477451

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033370
dbSNP (classic)	rs111033370
ClinGen	rs111033370
ebi	rs111033370
HLI	rs111033370
Exac	rs111033370
Gnomad	rs111033370
Varsome	rs111033370
LitVar	rs111033370
Map	rs111033370
PheGenI	rs111033370
Biobank	rs111033370
1000 genomes	rs111033370
hgdp	rs111033370
ensembl	rs111033370
geneview	rs111033370
scholar	rs111033370
google	rs111033370
pharmgkb	rs111033370
gwascentral	rs111033370
openSNP	rs111033370
23andMe	rs111033370
SNPshot	rs111033370
SNPdbe	rs111033370
MSV3d	rs111033370
GWAS Ctlg	rs111033370

Max Magnitude

0

ClinVar
Risk	rs111033370(A;A)
Alt	rs111033370(A;A)
Reference	Rs111033370(;)
Significance	Probable-Pathogenic
Disease	Non-syndromic genetic deafness
Variation	info
Gene	OTOF
CLNDBN	Non-syndromic genetic deafness
Reversed	1
HGVS	NC_000002.11:g.26700319_26700320insT
CLNSRC	ClinVar
CLNACC	RCV000041491.2,