rs397515610

Orientation

minus

Stabilized

minus

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

Make rs397515610(C;T)

Make rs397515610(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26502301

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515610
dbSNP (classic)	rs397515610
ClinGen	rs397515610
ebi	rs397515610
HLI	rs397515610
Exac	rs397515610
Gnomad	rs397515610
Varsome	rs397515610
LitVar	rs397515610
Map	rs397515610
PheGenI	rs397515610
Biobank	rs397515610
1000 genomes	rs397515610
hgdp	rs397515610
ensembl	rs397515610
geneview	rs397515610
scholar	rs397515610
google	rs397515610
pharmgkb	rs397515610
gwascentral	rs397515610
openSNP	rs397515610
23andMe	rs397515610
SNPshot	rs397515610
SNPdbe	rs397515610
MSV3d	rs397515610
GWAS Ctlg	rs397515610

Max Magnitude

0

ClinVar
Risk	rs397515610(G;G) rs397515610(T;T)
Alt	rs397515610(G;G) rs397515610(T;T)
Reference	Rs397515610(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26725169G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000056054.1,