rs876657658

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AT;AT)	0	common in clinvar
(TA;TA)	0	common in clinvar

Make rs876657658(-;-)

Make rs876657658(-;AT)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

80238874

Gene

OTOGL

is a	snp
is	mentioned by
dbSNP	rs876657658
dbSNP (classic)	rs876657658
ClinGen	rs876657658
ebi	rs876657658
HLI	rs876657658
Exac	rs876657658
Gnomad	rs876657658
Varsome	rs876657658
LitVar	rs876657658
Map	rs876657658
PheGenI	rs876657658
Biobank	rs876657658
1000 genomes	rs876657658
hgdp	rs876657658
ensembl	rs876657658
geneview	rs876657658
scholar	rs876657658
google	rs876657658
pharmgkb	rs876657658
gwascentral	rs876657658
openSNP	rs876657658
23andMe	rs876657658
SNPshot	rs876657658
SNPdbe	rs876657658
MSV3d	rs876657658
GWAS Ctlg	rs876657658

Max Magnitude

0

ClinVar
Risk	rs876657658(-;-) Rs876657658(TA;TA)
Alt	rs876657658(-;-) Rs876657658(TA;TA)
Reference	Rs876657658(AT;AT)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	OTOGL
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000012.11:g.80632654_80632655delAT
CLNSRC
CLNACC	RCV000220106.1,