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rs281865525

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865525(-;-)
Make rs281865525(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position89178525
GeneTYR
is asnp
is mentioned by
dbSNPrs281865525
ebirs281865525
HLIrs281865525
Exacrs281865525
Varsomers281865525
Maprs281865525
PheGenIrs281865525
hapmaprs281865525
1000 genomesrs281865525
hgdprs281865525
ensemblrs281865525
gopubmedrs281865525
geneviewrs281865525
scholarrs281865525
googlers281865525
pharmgkbrs281865525
gwascentralrs281865525
openSNPrs281865525
23andMers281865525
23andMe allrs281865525
SNP Nexus

SNPshotrs281865525
SNPdbers281865525
MSV3drs281865525
GWAS Ctlgrs281865525
Max Magnitude0
ClinVar
Risk rs281865525(;)
Alt rs281865525(;)
Reference rs281865525(G;G)
Significance Pathogenic
Disease Tyrosinase-negative oculocutaneous albinism not provided
Variation info
Gene TYR
CLNDBN Tyrosinase-negative oculocutaneous albinism not provided
Reversed 0
HGVS NC_000011.9:g.88911693delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000003988.2, RCV000085954.1,