rs397515600

Orientation

minus

Stabilized

minus

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

Make rs397515600(C;T)

Make rs397515600(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26467435

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515600
dbSNP (classic)	rs397515600
ClinGen	rs397515600
ebi	rs397515600
HLI	rs397515600
Exac	rs397515600
Gnomad	rs397515600
Varsome	rs397515600
LitVar	rs397515600
Map	rs397515600
PheGenI	rs397515600
Biobank	rs397515600
1000 genomes	rs397515600
hgdp	rs397515600
ensembl	rs397515600
geneview	rs397515600
scholar	rs397515600
google	rs397515600
pharmgkb	rs397515600
gwascentral	rs397515600
openSNP	rs397515600
23andMe	rs397515600
SNPshot	rs397515600
SNPdbe	rs397515600
MSV3d	rs397515600
GWAS Ctlg	rs397515600

Max Magnitude

0

ClinVar
Risk	rs397515600(G;G) rs397515600(T;T)
Alt	rs397515600(G;G) rs397515600(T;T)
Reference	Rs397515600(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26690303G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000056040.1,