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rs797046082

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797046082(A;G)
Make rs797046082(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position89178399
GeneTYR
is asnp
is mentioned by
dbSNPrs797046082
ebirs797046082
HLIrs797046082
Exacrs797046082
Varsomers797046082
Maprs797046082
PheGenIrs797046082
hapmaprs797046082
1000 genomesrs797046082
hgdprs797046082
ensemblrs797046082
gopubmedrs797046082
geneviewrs797046082
scholarrs797046082
googlers797046082
pharmgkbrs797046082
gwascentralrs797046082
openSNPrs797046082
23andMers797046082
23andMe allrs797046082
SNP Nexus

SNPshotrs797046082
SNPdbers797046082
MSV3drs797046082
GWAS Ctlgrs797046082
Max Magnitude0
ClinVar
Risk rs797046082(G;G)
Alt rs797046082(G;G)
Reference rs797046082(A;A)
Significance Probable-Pathogenic
Disease Tyrosinase-negative oculocutaneous albinism
Variation info
Gene TYR
CLNDBN Tyrosinase-negative oculocutaneous albinism
Reversed 0
HGVS NC_000011.9:g.88911567A>G
CLNSRC
CLNACC RCV000195203.1,