rs1060499804

Orientation

plus

Stabilized

plus

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

Make rs1060499804(A;T)

Make rs1060499804(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

21705213

Gene

OTOA

is a	snp
is	mentioned by
dbSNP	rs1060499804
dbSNP (classic)	rs1060499804
ClinGen	rs1060499804
ebi	rs1060499804
HLI	rs1060499804
Exac	rs1060499804
Gnomad	rs1060499804
Varsome	rs1060499804
LitVar	rs1060499804
Map	rs1060499804
PheGenI	rs1060499804
Biobank	rs1060499804
1000 genomes	rs1060499804
hgdp	rs1060499804
ensembl	rs1060499804
geneview	rs1060499804
scholar	rs1060499804
google	rs1060499804
pharmgkb	rs1060499804
gwascentral	rs1060499804
openSNP	rs1060499804
23andMe	rs1060499804
SNPshot	rs1060499804
SNPdbe	rs1060499804
MSV3d	rs1060499804
GWAS Ctlg	rs1060499804

Max Magnitude

0

ClinVar
Risk	rs1060499804(T;T)
Alt	rs1060499804(T;T)
Reference	Rs1060499804(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOA
CLNDBN	Deafness, autosomal recessive 22
Reversed	0
HGVS	NC_000016.9:g.21716534A>T
CLNSRC
CLNACC	RCV000454173.1,