rs1060499786

Orientation

plus

Stabilized

plus

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

Make rs1060499786(-;-)

Make rs1060499786(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

21697863

Gene

OTOA

is a	snp
is	mentioned by
dbSNP	rs1060499786
dbSNP (classic)	rs1060499786
ClinGen	rs1060499786
ebi	rs1060499786
HLI	rs1060499786
Exac	rs1060499786
Gnomad	rs1060499786
Varsome	rs1060499786
LitVar	rs1060499786
Map	rs1060499786
PheGenI	rs1060499786
Biobank	rs1060499786
1000 genomes	rs1060499786
hgdp	rs1060499786
ensembl	rs1060499786
geneview	rs1060499786
scholar	rs1060499786
google	rs1060499786
pharmgkb	rs1060499786
gwascentral	rs1060499786
openSNP	rs1060499786
23andMe	rs1060499786
SNPshot	rs1060499786
SNPdbe	rs1060499786
MSV3d	rs1060499786
GWAS Ctlg	rs1060499786

Max Magnitude

0

ClinVar
Risk	rs1060499786(-;-)
Alt	rs1060499786(-;-)
Reference	Rs1060499786(T;T)
Significance	Probable-Pathogenic
Disease	Deafness
Variation	info
Gene	OTOA
CLNDBN	Deafness, autosomal recessive 22
Reversed	0
HGVS	NC_000016.9:g.21709184delT
CLNSRC
CLNACC	RCV000454262.1,