rs397515586

Orientation

minus

Stabilized

minus

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

Make rs397515586(G;G)

Make rs397515586(G;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26480871

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515586
dbSNP (classic)	rs397515586
ClinGen	rs397515586
ebi	rs397515586
HLI	rs397515586
Exac	rs397515586
Gnomad	rs397515586
Varsome	rs397515586
LitVar	rs397515586
Map	rs397515586
PheGenI	rs397515586
Biobank	rs397515586
1000 genomes	rs397515586
hgdp	rs397515586
ensembl	rs397515586
geneview	rs397515586
scholar	rs397515586
google	rs397515586
pharmgkb	rs397515586
gwascentral	rs397515586
openSNP	rs397515586
23andMe	rs397515586
SNPshot	rs397515586
SNPdbe	rs397515586
MSV3d	rs397515586
GWAS Ctlg	rs397515586

Max Magnitude

0

ClinVar
Risk	rs397515586(G;G)
Alt	rs397515586(G;G)
Reference	Rs397515586(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26703739A>C
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000056020.1,