rs370730786

Orientation

plus

Stabilized

plus

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

Make rs370730786(A;A)

Make rs370730786(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

80302784

Gene

OTOGL

is a	snp
is	mentioned by
dbSNP	rs370730786
dbSNP (classic)	rs370730786
ClinGen	rs370730786
ebi	rs370730786
HLI	rs370730786
Exac	rs370730786
Gnomad	rs370730786
Varsome	rs370730786
LitVar	rs370730786
Map	rs370730786
PheGenI	rs370730786
Biobank	rs370730786
1000 genomes	rs370730786
hgdp	rs370730786
ensembl	rs370730786
geneview	rs370730786
scholar	rs370730786
google	rs370730786
pharmgkb	rs370730786
gwascentral	rs370730786
openSNP	rs370730786
23andMe	rs370730786
SNPshot	rs370730786
SNPdbe	rs370730786
MSV3d	rs370730786
GWAS Ctlg	rs370730786

Max Magnitude

0

ClinVar
Risk	rs370730786(A;A)
Alt	rs370730786(A;A)
Reference	Rs370730786(G;G)
Significance	Probable-Pathogenic
Disease	Deafness
Variation	info
Gene	OTOGL
CLNDBN	Deafness, autosomal recessive 84b
Reversed	0
HGVS	NC_000012.11:g.80696564G>A
CLNSRC
CLNACC	RCV000373203.1,