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rs1057518763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518763(-;T)
Make rs1057518763(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position89178027
GeneLOC107984363, TYR
is asnp
is mentioned by
dbSNPrs1057518763
dbSNP (old)rs1057518763
ClinGenrs1057518763
ebirs1057518763
HLIrs1057518763
Exacrs1057518763
Gnomadrs1057518763
Varsomers1057518763
LitVarrs1057518763
Maprs1057518763
PheGenIrs1057518763
Biobankrs1057518763
1000 genomesrs1057518763
hgdprs1057518763
ensemblrs1057518763
gopubmedrs1057518763
geneviewrs1057518763
scholarrs1057518763
googlers1057518763
pharmgkbrs1057518763
gwascentralrs1057518763
openSNPrs1057518763
23andMers1057518763
23andMe allrs1057518763
SNPshotrs1057518763
SNPdbers1057518763
MSV3drs1057518763
GWAS Ctlgrs1057518763
Max Magnitude0
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,