rs3763317
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3763317(C;C) |
Make rs3763317(C;T) |
Make rs3763317(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32409011 |
Gene | BTNL2 |
is a | snp |
is | mentioned by |
dbSNP | rs3763317 |
dbSNP (classic) | rs3763317 |
ClinGen | rs3763317 |
ebi | rs3763317 |
HLI | rs3763317 |
Exac | rs3763317 |
Gnomad | rs3763317 |
Varsome | rs3763317 |
LitVar | rs3763317 |
Map | rs3763317 |
PheGenI | rs3763317 |
Biobank | rs3763317 |
1000 genomes | rs3763317 |
hgdp | rs3763317 |
ensembl | rs3763317 |
geneview | rs3763317 |
scholar | rs3763317 |
rs3763317 | |
pharmgkb | rs3763317 |
gwascentral | rs3763317 |
openSNP | rs3763317 |
23andMe | rs3763317 |
SNPshot | rs3763317 |
SNPdbe | rs3763317 |
MSV3d | rs3763317 |
GWAS Ctlg | rs3763317 |
GMAF | 0.4522 |
Max Magnitude | 0 |
? | (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 23028341] |
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 26617759] Association of genetic polymorphisms on BTNL2 with susceptibility to and prognosis of dilated cardiomyopathy in a Chinese population.