rs61753178

Orientation

plus

Stabilized

plus

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

Make rs61753178(C;T)

Make rs61753178(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

89178014

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs61753178
dbSNP (classic)	rs61753178
ClinGen	rs61753178
ebi	rs61753178
HLI	rs61753178
Exac	rs61753178
Gnomad	rs61753178
Varsome	rs61753178
LitVar	rs61753178
Map	rs61753178
PheGenI	rs61753178
Biobank	rs61753178
1000 genomes	rs61753178
hgdp	rs61753178
ensembl	rs61753178
geneview	rs61753178
scholar	rs61753178
google	rs61753178
pharmgkb	rs61753178
gwascentral	rs61753178
openSNP	rs61753178
23andMe	rs61753178
SNPshot	rs61753178
SNPdbe	rs61753178
MSV3d	rs61753178
GWAS Ctlg	rs61753178

Max Magnitude

0

OMIM	606933
Desc
Variant	0023
Related	also

ClinVar
Risk	rs61753178(T;T)
Alt	rs61753178(T;T)
Reference	Rs61753178(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.88911182C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003996.2, RCV000085959.1,