rs397515607

Orientation

minus

Stabilized

minus

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

Make rs397515607(-;-)

Make rs397515607(-;GAG)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26461817

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515607
dbSNP (classic)	rs397515607
ClinGen	rs397515607
ebi	rs397515607
HLI	rs397515607
Exac	rs397515607
Gnomad	rs397515607
Varsome	rs397515607
LitVar	rs397515607
Map	rs397515607
PheGenI	rs397515607
Biobank	rs397515607
1000 genomes	rs397515607
hgdp	rs397515607
ensembl	rs397515607
geneview	rs397515607
scholar	rs397515607
google	rs397515607
pharmgkb	rs397515607
gwascentral	rs397515607
openSNP	rs397515607
23andMe	rs397515607
SNPshot	rs397515607
SNPdbe	rs397515607
MSV3d	rs397515607
GWAS Ctlg	rs397515607

Max Magnitude

0

ClinVar
Risk	rs397515607(-;-)
Alt	rs397515607(-;-)
Reference	Rs397515607(GAG;GAG)
Significance	Other
Disease	Deafness Nonsyndromic hearing loss and deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9 Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000002.11:g.26684685_26684687delCTC
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000056050.6, RCV000211735.1,