rs606231140

Merged into

rs61754368

Orientation

plus

Stabilized

plus

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

Make rs606231140(-;-)

Make rs606231140(-;TG)

Make rs606231140(TG;TG)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

89178685

Gene

TYR

is a	snp
is	mentioned by
dbSNP	rs606231140
dbSNP (classic)	rs606231140
ClinGen	rs606231140
ebi	rs606231140
HLI	rs606231140
Exac	rs606231140
Gnomad	rs606231140
Varsome	rs606231140
LitVar	rs606231140
Map	rs606231140
PheGenI	rs606231140
Biobank	rs606231140
1000 genomes	rs606231140
hgdp	rs606231140
ensembl	rs606231140
geneview	rs606231140
scholar	rs606231140
google	rs606231140
pharmgkb	rs606231140
gwascentral	rs606231140
openSNP	rs606231140
23andMe	rs606231140
SNPshot	rs606231140
SNPdbe	rs606231140
MSV3d	rs606231140
GWAS Ctlg	rs606231140

Status

Merged into rs61754368

Max Magnitude

0

ClinVar
Risk	rs606231140(TACAGCACA;TACAGCACA) rs606231140(TTG;TTG)
Alt	rs606231140(TACAGCACA;TACAGCACA) rs606231140(TTG;TTG)
Reference	Rs606231140(GT;GT)
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,