rs111033341

Orientation

minus

Stabilized

minus

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

Make rs111033341(G;G)

Make rs111033341(G;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26489209

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs111033341
dbSNP (classic)	rs111033341
ClinGen	rs111033341
ebi	rs111033341
HLI	rs111033341
Exac	rs111033341
Gnomad	rs111033341
Varsome	rs111033341
LitVar	rs111033341
Map	rs111033341
PheGenI	rs111033341
Biobank	rs111033341
1000 genomes	rs111033341
hgdp	rs111033341
ensembl	rs111033341
geneview	rs111033341
scholar	rs111033341
google	rs111033341
pharmgkb	rs111033341
gwascentral	rs111033341
openSNP	rs111033341
23andMe	rs111033341
SNPshot	rs111033341
SNPdbe	rs111033341
MSV3d	rs111033341
GWAS Ctlg	rs111033341

Max Magnitude

0

ClinVar
Risk	rs111033341(G;G)
Alt	rs111033341(G;G)
Reference	Rs111033341(T;T)
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.26712077A>C
CLNSRC	ClinVar
CLNACC	RCV000041453.2,