rs367543066

Orientation

plus

Stabilized

plus

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

Make rs367543066(C;G)

Make rs367543066(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

89178504

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs367543066
dbSNP (classic)	rs367543066
ClinGen	rs367543066
ebi	rs367543066
HLI	rs367543066
Exac	rs367543066
Gnomad	rs367543066
Varsome	rs367543066
LitVar	rs367543066
Map	rs367543066
PheGenI	rs367543066
Biobank	rs367543066
1000 genomes	rs367543066
hgdp	rs367543066
ensembl	rs367543066
geneview	rs367543066
scholar	rs367543066
google	rs367543066
pharmgkb	rs367543066
gwascentral	rs367543066
openSNP	rs367543066
23andMe	rs367543066
SNPshot	rs367543066
SNPdbe	rs367543066
MSV3d	rs367543066
GWAS Ctlg	rs367543066

Max Magnitude

0

ClinVar
Risk	rs367543066(G;G) rs367543066(T;T)
Alt	rs367543066(G;G) rs367543066(T;T)
Reference	Rs367543066(C;C)
Significance	Probable-Pathogenic
Disease	Oculocutaneous albinism type 1B Tyrosinase-negative oculocutaneous albinism
Variation	info
Gene	TYR
CLNDBN	Oculocutaneous albinism type 1B Tyrosinase-negative oculocutaneous albinism
Reversed	0
HGVS	NC_000011.9:g.88911672C>G
CLNSRC	ClinVar
CLNACC	RCV000133602.1,