rs397515588

Orientation

minus

Stabilized

minus

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

Make rs397515588(A;A)

Make rs397515588(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26480809

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515588
dbSNP (classic)	rs397515588
ClinGen	rs397515588
ebi	rs397515588
HLI	rs397515588
Exac	rs397515588
Gnomad	rs397515588
Varsome	rs397515588
LitVar	rs397515588
Map	rs397515588
PheGenI	rs397515588
Biobank	rs397515588
1000 genomes	rs397515588
hgdp	rs397515588
ensembl	rs397515588
geneview	rs397515588
scholar	rs397515588
google	rs397515588
pharmgkb	rs397515588
gwascentral	rs397515588
openSNP	rs397515588
23andMe	rs397515588
SNPshot	rs397515588
SNPdbe	rs397515588
MSV3d	rs397515588
GWAS Ctlg	rs397515588

Max Magnitude

0

ClinVar
Risk	rs397515588(A;A)
Alt	rs397515588(A;A)
Reference	Rs397515588(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26703677C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000056022.1,