rs794727898

Orientation

minus

Stabilized

minus

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

Make rs794727898(-;-)

Make rs794727898(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

28016127

Gene

OCA2

is a	snp
is	mentioned by
dbSNP	rs794727898
dbSNP (classic)	rs794727898
ClinGen	rs794727898
ebi	rs794727898
HLI	rs794727898
Exac	rs794727898
Gnomad	rs794727898
Varsome	rs794727898
LitVar	rs794727898
Map	rs794727898
PheGenI	rs794727898
Biobank	rs794727898
1000 genomes	rs794727898
hgdp	rs794727898
ensembl	rs794727898
geneview	rs794727898
scholar	rs794727898
google	rs794727898
pharmgkb	rs794727898
gwascentral	rs794727898
openSNP	rs794727898
23andMe	rs794727898
SNPshot	rs794727898
SNPdbe	rs794727898
MSV3d	rs794727898
GWAS Ctlg	rs794727898

Max Magnitude

0

ClinVar
Risk	rs794727898(-;-)
Alt	rs794727898(-;-)
Reference	Rs794727898(C;C)
Significance	Pathogenic
Disease	Tyrosinase-positive oculocutaneous albinism
Variation	info
Gene	OCA2
CLNDBN	Tyrosinase-positive oculocutaneous albinism
Reversed	1
HGVS	NC_000015.9:g.28261273delG
CLNSRC
CLNACC	RCV000180124.1,