rs797045839

Orientation

minus

Stabilized

minus

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

Make rs797045839(A;A)

Make rs797045839(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

27845047

Gene

OCA2

is a	snp
is	mentioned by
dbSNP	rs797045839
dbSNP (classic)	rs797045839
ClinGen	rs797045839
ebi	rs797045839
HLI	rs797045839
Exac	rs797045839
Gnomad	rs797045839
Varsome	rs797045839
LitVar	rs797045839
Map	rs797045839
PheGenI	rs797045839
Biobank	rs797045839
1000 genomes	rs797045839
hgdp	rs797045839
ensembl	rs797045839
geneview	rs797045839
scholar	rs797045839
google	rs797045839
pharmgkb	rs797045839
gwascentral	rs797045839
openSNP	rs797045839
23andMe	rs797045839
SNPshot	rs797045839
SNPdbe	rs797045839
MSV3d	rs797045839
GWAS Ctlg	rs797045839

Max Magnitude

0

ClinVar
Risk	rs797045839(A;A)
Alt	rs797045839(A;A)
Reference	Rs797045839(G;G)
Significance	Probable-Pathogenic
Disease	Tyrosinase-positive oculocutaneous albinism
Variation	info
Gene	OCA2
CLNDBN	Tyrosinase-positive oculocutaneous albinism
Reversed	1
HGVS	NC_000015.9:g.28090193C>T
CLNSRC
CLNACC	RCV000193498.1,