rs397515587

Orientation

minus

Stabilized

minus

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

Make rs397515587(-;-)

Make rs397515587(-;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26480849

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515587
dbSNP (classic)	rs397515587
ClinGen	rs397515587
ebi	rs397515587
HLI	rs397515587
Exac	rs397515587
Gnomad	rs397515587
Varsome	rs397515587
LitVar	rs397515587
Map	rs397515587
PheGenI	rs397515587
Biobank	rs397515587
1000 genomes	rs397515587
hgdp	rs397515587
ensembl	rs397515587
geneview	rs397515587
scholar	rs397515587
google	rs397515587
pharmgkb	rs397515587
gwascentral	rs397515587
openSNP	rs397515587
23andMe	rs397515587
SNPshot	rs397515587
SNPdbe	rs397515587
MSV3d	rs397515587
GWAS Ctlg	rs397515587

Max Magnitude

0

ClinVar
Risk	rs397515587(-;-)
Alt	rs397515587(-;-)
Reference	Rs397515587(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26703717delG
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000056021.1,