rs770917728

Orientation

plus

Stabilized

plus

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

Make rs770917728(C;G)

Make rs770917728(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

80279091

Gene

OTOGL

is a	snp
is	mentioned by
dbSNP	rs770917728
dbSNP (classic)	rs770917728
ClinGen	rs770917728
ebi	rs770917728
HLI	rs770917728
Exac	rs770917728
Gnomad	rs770917728
Varsome	rs770917728
LitVar	rs770917728
Map	rs770917728
PheGenI	rs770917728
Biobank	rs770917728
1000 genomes	rs770917728
hgdp	rs770917728
ensembl	rs770917728
geneview	rs770917728
scholar	rs770917728
google	rs770917728
pharmgkb	rs770917728
gwascentral	rs770917728
openSNP	rs770917728
23andMe	rs770917728
SNPshot	rs770917728
SNPdbe	rs770917728
MSV3d	rs770917728
GWAS Ctlg	rs770917728

Max Magnitude

0

ClinVar
Risk	rs770917728(G;G) rs770917728(T;T)
Alt	rs770917728(G;G) rs770917728(T;T)
Reference	Rs770917728(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	OTOGL
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.80672871C>G
CLNSRC
CLNACC	RCV000478691.1,