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rs383592

From SNPedia

Orientationplus
Make rs383592(C;C)
Make rs383592(C;T)
Make rs383592(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89792100
is asnp
is mentioned by
dbSNPrs383592
ebirs383592
HLIrs383592
Exacrs383592
Varsomers383592
Maprs383592
PheGenIrs383592
hapmaprs383592
1000 genomesrs383592
hgdprs383592
ensemblrs383592
gopubmedrs383592
geneviewrs383592
scholarrs383592
googlers383592
pharmgkbrs383592
gwascentralrs383592
openSNPrs383592
23andMers383592
23andMe allrs383592
SNP Nexus

SNPshotrs383592
SNPdbers383592
MSV3drs383592
GWAS Ctlgrs383592
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25642632] Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy.