rs3811140
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3811140(C;C) |
Make rs3811140(C;T) |
Make rs3811140(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 134880265 |
Gene | FCN2 |
is a | snp |
is | mentioned by |
dbSNP | rs3811140 |
dbSNP (classic) | rs3811140 |
ClinGen | rs3811140 |
ebi | rs3811140 |
HLI | rs3811140 |
Exac | rs3811140 |
Gnomad | rs3811140 |
Varsome | rs3811140 |
LitVar | rs3811140 |
Map | rs3811140 |
PheGenI | rs3811140 |
Biobank | rs3811140 |
1000 genomes | rs3811140 |
hgdp | rs3811140 |
ensembl | rs3811140 |
geneview | rs3811140 |
scholar | rs3811140 |
rs3811140 | |
pharmgkb | rs3811140 |
gwascentral | rs3811140 |
openSNP | rs3811140 |
23andMe | rs3811140 |
SNPshot | rs3811140 |
SNPdbe | rs3811140 |
MSV3d | rs3811140 |
GWAS Ctlg | rs3811140 |
GMAF | 0.1635 |
Max Magnitude | 0 |
[PMID 23423485] Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China [PMID 23525825] Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.