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rs77061563

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs77061563(C;T)
Make rs77061563(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position11358685
GeneLOC105371082
is asnp
is mentioned by
dbSNPrs77061563
dbSNP (classic)rs77061563
ClinGenrs77061563
ebirs77061563
HLIrs77061563
Exacrs77061563
Gnomadrs77061563
Varsomers77061563
LitVarrs77061563
Maprs77061563
PheGenIrs77061563
Biobankrs77061563
1000 genomesrs77061563
hgdprs77061563
ensemblrs77061563
geneviewrs77061563
scholarrs77061563
googlers77061563
pharmgkbrs77061563
gwascentralrs77061563
openSNPrs77061563
23andMers77061563
SNPshotrs77061563
SNPdbers77061563
MSV3drs77061563
GWAS Ctlgrs77061563
Max Magnitude0

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