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rs797046081

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797046081(C;G)
Make rs797046081(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position89284822
GeneTYR
is asnp
is mentioned by
dbSNPrs797046081
ebirs797046081
HLIrs797046081
Exacrs797046081
Varsomers797046081
Maprs797046081
PheGenIrs797046081
hapmaprs797046081
1000 genomesrs797046081
hgdprs797046081
ensemblrs797046081
gopubmedrs797046081
geneviewrs797046081
scholarrs797046081
googlers797046081
pharmgkbrs797046081
gwascentralrs797046081
openSNPrs797046081
23andMers797046081
23andMe allrs797046081
SNP Nexus

SNPshotrs797046081
SNPdbers797046081
MSV3drs797046081
GWAS Ctlgrs797046081
Max Magnitude0
ClinVar
Risk rs797046081(G;G)
Alt rs797046081(G;G)
Reference rs797046081(C;C)
Significance Probable-Pathogenic
Disease Tyrosinase-negative oculocutaneous albinism
Variation info
Gene TYR
CLNDBN Tyrosinase-negative oculocutaneous albinism
Reversed 0
HGVS NC_000011.9:g.89017990C>G
CLNSRC
CLNACC RCV000195133.1,