rs61753184

Orientation

plus

Stabilized

plus

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

Make rs61753184(C;T)

Make rs61753184(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

89178182

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs61753184
dbSNP (classic)	rs61753184
ClinGen	rs61753184
ebi	rs61753184
HLI	rs61753184
Exac	rs61753184
Gnomad	rs61753184
Varsome	rs61753184
LitVar	rs61753184
Map	rs61753184
PheGenI	rs61753184
Biobank	rs61753184
1000 genomes	rs61753184
hgdp	rs61753184
ensembl	rs61753184
geneview	rs61753184
scholar	rs61753184
google	rs61753184
pharmgkb	rs61753184
gwascentral	rs61753184
openSNP	rs61753184
23andMe	rs61753184
SNPshot	rs61753184
SNPdbe	rs61753184
MSV3d	rs61753184
GWAS Ctlg	rs61753184

Max Magnitude

0

ClinVar
Risk	rs61753184(T;T)
Alt	rs61753184(T;T)
Reference	Rs61753184(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.88911350C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000085933.1, RCV000414815.1,