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rs2076533

From SNPedia

Orientationminus
Stabilizedminus
Make rs2076533(A;A)
Make rs2076533(A;G)
Make rs2076533(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32395750
GeneBTNL2, LOC101929163
is asnp
is mentioned by
dbSNPrs2076533
dbSNP (classic)rs2076533
ClinGenrs2076533
ebirs2076533
HLIrs2076533
Exacrs2076533
Gnomadrs2076533
Varsomers2076533
LitVarrs2076533
Maprs2076533
PheGenIrs2076533
Biobankrs2076533
1000 genomesrs2076533
hgdprs2076533
ensemblrs2076533
geneviewrs2076533
scholarrs2076533
googlers2076533
pharmgkbrs2076533
gwascentralrs2076533
openSNPrs2076533
23andMers2076533
SNPshotrs2076533
SNPdbers2076533
MSV3drs2076533
GWAS Ctlgrs2076533
GMAF0.365
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 22991420] Genetic characterization and susceptibility for sarcoidosis in Japanese patients: risk factors of BTNL2 gene polymorphisms and HLA class II alleles


[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.


[PMID 20018019OA-icon.png] Two-stage joint selection method to identify candidate markers from genome-wide association studies.