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rs3088362

From SNPedia

Orientationplus
Stabilizedplus
Make rs3088362(A;A)
Make rs3088362(A;C)
Make rs3088362(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position43859494
GeneCCDC122
is asnp
is mentioned by
dbSNPrs3088362
ebirs3088362
HLIrs3088362
Exacrs3088362
Varsomers3088362
Maprs3088362
PheGenIrs3088362
hapmaprs3088362
1000 genomesrs3088362
hgdprs3088362
ensemblrs3088362
gopubmedrs3088362
geneviewrs3088362
scholarrs3088362
googlers3088362
pharmgkbrs3088362
gwascentralrs3088362
openSNPrs3088362
23andMers3088362
23andMe allrs3088362
SNP Nexus

SNPshotrs3088362
SNPdbers3088362
MSV3drs3088362
GWAS Ctlgrs3088362
GMAF0.2034
Max Magnitude
? (A;A) (A;C) (C;C) 28
Variant in the CCDC122 region associated with increased susceptibility to leprosy in Asians, according to the 23andMe blog 23andMe's blog. The risk allele is A, and the odds ratio is 1.52.
OMIM613407
Desc
Variant
Relatedalso