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rs796051878

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051878(A;A)
Make rs796051878(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position89178092
GeneTYR
is asnp
is mentioned by
dbSNPrs796051878
ebirs796051878
HLIrs796051878
Exacrs796051878
Varsomers796051878
Maprs796051878
PheGenIrs796051878
hapmaprs796051878
1000 genomesrs796051878
hgdprs796051878
ensemblrs796051878
gopubmedrs796051878
geneviewrs796051878
scholarrs796051878
googlers796051878
pharmgkbrs796051878
gwascentralrs796051878
openSNPrs796051878
23andMers796051878
23andMe allrs796051878
SNP Nexus

SNPshotrs796051878
SNPdbers796051878
MSV3drs796051878
GWAS Ctlgrs796051878
Max Magnitude0
ClinVar
Risk rs796051878(A;A)
Alt rs796051878(A;A)
Reference rs796051878(G;G)
Significance Probable-Pathogenic
Disease Tyrosinase-negative oculocutaneous albinism
Variation info
Gene TYR
CLNDBN Tyrosinase-negative oculocutaneous albinism
Reversed 0
HGVS NC_000011.9:g.88911260G>A
CLNSRC
CLNACC RCV000186573.1,