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rs998592

From SNPedia

Orientationminus
Stabilizedminus
Make rs998592(A;A)
Make rs998592(A;G)
Make rs998592(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position11105821
GeneCLEC16A
is asnp
is mentioned by
dbSNPrs998592
ebirs998592
HLIrs998592
Exacrs998592
Varsomers998592
Maprs998592
PheGenIrs998592
hapmaprs998592
1000 genomesrs998592
hgdprs998592
ensemblrs998592
gopubmedrs998592
geneviewrs998592
scholarrs998592
googlers998592
pharmgkbrs998592
gwascentralrs998592
openSNPrs998592
23andMers998592
23andMe allrs998592
SNP Nexus

SNPshotrs998592
SNPdbers998592
MSV3drs998592
GWAS Ctlgrs998592
GMAF0.348
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20849399] More CLEC16A gene variants associated with multiple sclerosis


[PMID 22534877] Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance