rs61754361

Orientation

plus

Stabilized

plus

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

Make rs61754361(-;-)

Make rs61754361(-;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

89178521

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs61754361
dbSNP (classic)	rs61754361
ClinGen	rs61754361
ebi	rs61754361
HLI	rs61754361
Exac	rs61754361
Gnomad	rs61754361
Varsome	rs61754361
LitVar	rs61754361
Map	rs61754361
PheGenI	rs61754361
Biobank	rs61754361
1000 genomes	rs61754361
hgdp	rs61754361
ensembl	rs61754361
geneview	rs61754361
scholar	rs61754361
google	rs61754361
pharmgkb	rs61754361
gwascentral	rs61754361
openSNP	rs61754361
23andMe	rs61754361
SNPshot	rs61754361
SNPdbe	rs61754361
MSV3d	rs61754361
GWAS Ctlg	rs61754361

Merged from

Rs281865525

Max Magnitude

0

OMIM	606933
Desc
Variant	0015
Related	also

ClinVar
Risk	rs61754361(-;-)
Alt	rs61754361(-;-)
Reference	Rs61754361(G;G)
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.88911693delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003988.2, RCV000085954.1,