rs281865328

Orientation

plus

Stabilized

plus

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

Make rs281865328(-;C)

Make rs281865328(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

89295277

Gene

TYR

is a	snp
is	mentioned by
dbSNP	rs281865328
dbSNP (classic)	rs281865328
ClinGen	rs281865328
ebi	rs281865328
HLI	rs281865328
Exac	rs281865328
Gnomad	rs281865328
Varsome	rs281865328
LitVar	rs281865328
Map	rs281865328
PheGenI	rs281865328
Biobank	rs281865328
1000 genomes	rs281865328
hgdp	rs281865328
ensembl	rs281865328
geneview	rs281865328
scholar	rs281865328
google	rs281865328
pharmgkb	rs281865328
gwascentral	rs281865328
openSNP	rs281865328
23andMe	rs281865328
SNPshot	rs281865328
SNPdbe	rs281865328
MSV3d	rs281865328
GWAS Ctlg	rs281865328

Max Magnitude

0

ClinVar
Risk	rs281865328(C;C)
Alt	rs281865328(C;C)
Reference	Rs281865328(-;-)
Significance	Pathogenic
Disease	Tyrosinase-negative oculocutaneous albinism not provided
Variation	info
Gene	TYR
CLNDBN	Tyrosinase-negative oculocutaneous albinism not provided
Reversed	0
HGVS	NC_000011.9:g.89028445dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004008.2, RCV000085928.1,