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rs3763317

From SNPedia

Orientationplus
Stabilizedplus
Make rs3763317(C;C)
Make rs3763317(C;T)
Make rs3763317(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32409011
GeneBTNL2
is asnp
is mentioned by
dbSNPrs3763317
ebirs3763317
HLIrs3763317
Exacrs3763317
Varsomers3763317
Maprs3763317
PheGenIrs3763317
hapmaprs3763317
1000 genomesrs3763317
hgdprs3763317
ensemblrs3763317
gopubmedrs3763317
geneviewrs3763317
scholarrs3763317
googlers3763317
pharmgkbrs3763317
gwascentralrs3763317
openSNPrs3763317
23andMers3763317
23andMe allrs3763317
SNP Nexus

SNPshotrs3763317
SNPdbers3763317
MSV3drs3763317
GWAS Ctlgrs3763317
GMAF0.4522
Max Magnitude
? (C;C) (C;T) (T;T) 28

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

GWAS snp
PMID [PMID 23028341OA-icon.png]
Trait Complement C3 and C4 levels
Title Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects.
Risk Allele C
P-val 9E-66
Odds Ratio .12 [0.10-0.14] g/L increase


[PMID 26617759OA-icon.png] Association of genetic polymorphisms on BTNL2 with susceptibility to and prognosis of dilated cardiomyopathy in a Chinese population.