rs61754365

Orientation

plus

Stabilized

plus

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

Make rs61754365(A;A)

Make rs61754365(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

89178603

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs61754365
dbSNP (classic)	rs61754365
ClinGen	rs61754365
ebi	rs61754365
HLI	rs61754365
Exac	rs61754365
Gnomad	rs61754365
Varsome	rs61754365
LitVar	rs61754365
Map	rs61754365
PheGenI	rs61754365
Biobank	rs61754365
1000 genomes	rs61754365
hgdp	rs61754365
ensembl	rs61754365
geneview	rs61754365
scholar	rs61754365
google	rs61754365
pharmgkb	rs61754365
gwascentral	rs61754365
openSNP	rs61754365
23andMe	rs61754365
SNPshot	rs61754365
SNPdbe	rs61754365
MSV3d	rs61754365
GWAS Ctlg	rs61754365

Max Magnitude

0

ClinVar
Risk	rs61754365(A;A) rs61754365(T;T)
Alt	rs61754365(A;A) rs61754365(T;T)
Reference	Rs61754365(G;G)
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.88911771G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000085964.1, RCV000194283.1,