rs1057518763

Orientation

plus

Stabilized

plus

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

Make rs1057518763(-;T)

Make rs1057518763(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

89178027

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs1057518763
dbSNP (classic)	rs1057518763
ClinGen	rs1057518763
ebi	rs1057518763
HLI	rs1057518763
Exac	rs1057518763
Gnomad	rs1057518763
Varsome	rs1057518763
LitVar	rs1057518763
Map	rs1057518763
PheGenI	rs1057518763
Biobank	rs1057518763
1000 genomes	rs1057518763
hgdp	rs1057518763
ensembl	rs1057518763
geneview	rs1057518763
scholar	rs1057518763
google	rs1057518763
pharmgkb	rs1057518763
gwascentral	rs1057518763
openSNP	rs1057518763
23andMe	rs1057518763
SNPshot	rs1057518763
SNPdbe	rs1057518763
MSV3d	rs1057518763
GWAS Ctlg	rs1057518763

Max Magnitude

0

ClinVar
Risk	rs1057518763(T;T)
Alt	rs1057518763(T;T)
Reference	Rs1057518763(-;-)
Significance	Pathogenic
Disease	Ocular albinism
Variation	info
Gene	TYR
CLNDBN	Ocular albinism
Reversed	0
HGVS	NC_000011.9:g.88911195dupT
CLNSRC
CLNACC	RCV000414891.1,