rs61754368

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GT;GT)	0	common in clinvar
(I;I)	0
(T;T)	0	common in clinvar
(TG;TG)	0	common in clinvar

Make rs61754368(-;-)

Make rs61754368(-;TG)

Reference

GRCh38 38.1/142

Chromosome

11

Position

89178683

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs61754368
dbSNP (classic)	rs61754368
ClinGen	rs61754368
ebi	rs61754368
HLI	rs61754368
Exac	rs61754368
Gnomad	rs61754368
Varsome	rs61754368
LitVar	rs61754368
Map	rs61754368
PheGenI	rs61754368
Biobank	rs61754368
1000 genomes	rs61754368
hgdp	rs61754368
ensembl	rs61754368
geneview	rs61754368
scholar	rs61754368
google	rs61754368
pharmgkb	rs61754368
gwascentral	rs61754368
openSNP	rs61754368
23andMe	rs61754368
SNPshot	rs61754368
SNPdbe	rs61754368
MSV3d	rs61754368
GWAS Ctlg	rs61754368

Merged from

Rs606231140

Max Magnitude

0

ClinVar
Risk	rs61754368(-;-) Rs61754368(GT;GT)
Alt	rs61754368(-;-) Rs61754368(GT;GT)
Reference	Rs61754368(TG;TG)
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.88911853_88911854delTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003990.2, RCV000085968.1,