rs397515589

Orientation

minus

Stabilized

minus

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

Make rs397515589(A;A)

Make rs397515589(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26480274

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515589
dbSNP (classic)	rs397515589
ClinGen	rs397515589
ebi	rs397515589
HLI	rs397515589
Exac	rs397515589
Gnomad	rs397515589
Varsome	rs397515589
LitVar	rs397515589
Map	rs397515589
PheGenI	rs397515589
Biobank	rs397515589
1000 genomes	rs397515589
hgdp	rs397515589
ensembl	rs397515589
geneview	rs397515589
scholar	rs397515589
google	rs397515589
pharmgkb	rs397515589
gwascentral	rs397515589
openSNP	rs397515589
23andMe	rs397515589
SNPshot	rs397515589
SNPdbe	rs397515589
MSV3d	rs397515589
GWAS Ctlg	rs397515589

Max Magnitude

0

ClinVar
Risk	rs397515589(A;A)
Alt	rs397515589(A;A)
Reference	Rs397515589(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26703142C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000056023.1,