rs61754371

Orientation

plus

Stabilized

plus

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

Make rs61754371(C;G)

Make rs61754371(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

89191199

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs61754371
dbSNP (classic)	rs61754371
ClinGen	rs61754371
ebi	rs61754371
HLI	rs61754371
Exac	rs61754371
Gnomad	rs61754371
Varsome	rs61754371
LitVar	rs61754371
Map	rs61754371
PheGenI	rs61754371
Biobank	rs61754371
1000 genomes	rs61754371
hgdp	rs61754371
ensembl	rs61754371
geneview	rs61754371
scholar	rs61754371
google	rs61754371
pharmgkb	rs61754371
gwascentral	rs61754371
openSNP	rs61754371
23andMe	rs61754371
SNPshot	rs61754371
SNPdbe	rs61754371
MSV3d	rs61754371
GWAS Ctlg	rs61754371

Max Magnitude

0

ClinVar
Risk	rs61754371(G;G)
Alt	rs61754371(G;G)
Reference	Rs61754371(C;C)
Significance	Pathogenic
Disease	not provided Tyrosinase-negative oculocutaneous albinism
Variation	info
Gene	TYR
CLNDBN	not provided Tyrosinase-negative oculocutaneous albinism
Reversed	0
HGVS	NC_000011.9:g.88924367C>G
CLNSRC
CLNACC	RCV000085972.1, RCV000194448.1,