rs137854890

Orientation

plus

Stabilized

plus

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

Make rs137854890(A;A)

Make rs137854890(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

89178225

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs137854890
dbSNP (classic)	rs137854890
ClinGen	rs137854890
ebi	rs137854890
HLI	rs137854890
Exac	rs137854890
Gnomad	rs137854890
Varsome	rs137854890
LitVar	rs137854890
Map	rs137854890
PheGenI	rs137854890
Biobank	rs137854890
1000 genomes	rs137854890
hgdp	rs137854890
ensembl	rs137854890
geneview	rs137854890
scholar	rs137854890
google	rs137854890
pharmgkb	rs137854890
gwascentral	rs137854890
openSNP	rs137854890
23andMe	rs137854890
SNPshot	rs137854890
SNPdbe	rs137854890
MSV3d	rs137854890
GWAS Ctlg	rs137854890

Max Magnitude

0

ClinVar
Risk	rs137854890(A;A)
Alt	rs137854890(A;A)
Reference	Rs137854890(G;G)
Significance	Pathogenic
Disease	Tyrosinase-negative oculocutaneous albinism
Variation	info
Gene	TYR
CLNDBN	Tyrosinase-negative oculocutaneous albinism
Reversed	0
HGVS	NC_000011.9:g.88911393G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000033111.2,