rs13031859

Orientation

plus

Stabilized

plus

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

Make rs13031859(A;A)

Make rs13031859(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26519093

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs13031859
dbSNP (classic)	rs13031859
ClinGen	rs13031859
ebi	rs13031859
HLI	rs13031859
Exac	rs13031859
Gnomad	rs13031859
Varsome	rs13031859
LitVar	rs13031859
Map	rs13031859
PheGenI	rs13031859
Biobank	rs13031859
1000 genomes	rs13031859
hgdp	rs13031859
ensembl	rs13031859
geneview	rs13031859
scholar	rs13031859
google	rs13031859
pharmgkb	rs13031859
gwascentral	rs13031859
openSNP	rs13031859
23andMe	rs13031859
SNPshot	rs13031859
SNPdbe	rs13031859
MSV3d	rs13031859
GWAS Ctlg	rs13031859

GMAF

0.281

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs13031859(A;A)
Alt	rs13031859(A;A)
Reference	Rs13031859(G;G)
Significance	Probable-non-pathogenic
Disease	Deafness not specified Nonsyndromic Hearing Loss
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9 not specified Nonsyndromic Hearing Loss, Recessive
Reversed	0
HGVS	NC_000002.11:g.26741961G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000021048.1, RCV000041497.3, RCV000367748.1,