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rs442309

From SNPedia

Orientationplus
Stabilizedplus
Make rs442309(C;C)
Make rs442309(C;T)
Make rs442309(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position62730735
is asnp
is mentioned by
dbSNPrs442309
ebirs442309
HLIrs442309
Exacrs442309
Varsomers442309
Maprs442309
PheGenIrs442309
hapmaprs442309
1000 genomesrs442309
hgdprs442309
ensemblrs442309
gopubmedrs442309
geneviewrs442309
scholarrs442309
googlers442309
pharmgkbrs442309
gwascentralrs442309
openSNPrs442309
23andMers442309
23andMe allrs442309
SNP Nexus

SNPshotrs442309
SNPdbers442309
MSV3drs442309
GWAS Ctlgrs442309
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25108386] Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3