rs104894315

Orientation

plus

Stabilized

plus

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

Make rs104894315(A;A)

Make rs104894315(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

89227932

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs104894315
dbSNP (classic)	rs104894315
ClinGen	rs104894315
ebi	rs104894315
HLI	rs104894315
Exac	rs104894315
Gnomad	rs104894315
Varsome	rs104894315
LitVar	rs104894315
Map	rs104894315
PheGenI	rs104894315
Biobank	rs104894315
1000 genomes	rs104894315
hgdp	rs104894315
ensembl	rs104894315
geneview	rs104894315
scholar	rs104894315
google	rs104894315
pharmgkb	rs104894315
gwascentral	rs104894315
openSNP	rs104894315
23andMe	rs104894315
SNPshot	rs104894315
SNPdbe	rs104894315
MSV3d	rs104894315
GWAS Ctlg	rs104894315

Max Magnitude

0

OMIM	606933
Desc
Variant	0016
Related	also

ClinVar
Risk	rs104894315(A;A) rs104894315(T;T)
Alt	rs104894315(A;A) rs104894315(T;T)
Reference	Rs104894315(C;C)
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.88961100C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003989.2, RCV000085902.1,