rs61754387

Orientation

plus

Stabilized

plus

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

Make rs61754387(A;C)

Make rs61754387(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

89227898

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs61754387
dbSNP (classic)	rs61754387
ClinGen	rs61754387
ebi	rs61754387
HLI	rs61754387
Exac	rs61754387
Gnomad	rs61754387
Varsome	rs61754387
LitVar	rs61754387
Map	rs61754387
PheGenI	rs61754387
Biobank	rs61754387
1000 genomes	rs61754387
hgdp	rs61754387
ensembl	rs61754387
geneview	rs61754387
scholar	rs61754387
google	rs61754387
pharmgkb	rs61754387
gwascentral	rs61754387
openSNP	rs61754387
23andMe	rs61754387
SNPshot	rs61754387
SNPdbe	rs61754387
MSV3d	rs61754387
GWAS Ctlg	rs61754387

Max Magnitude

0

OMIM	606933
Desc
Variant	0028
Related	also

ClinVar
Risk	rs61754387(C;C)
Alt	rs61754387(C;C)
Reference	Rs61754387(A;A)
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.88961066A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004002.2, RCV000085897.1,