rs2099902
From SNPedia
Orientation | plus |
Make rs2099902(C;C) |
Make rs2099902(C;T) |
Make rs2099902(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 10 |
Position | 52766089 |
Gene | LOC105378305, MBL2 |
is a | snp |
is | mentioned by |
dbSNP | rs2099902 |
dbSNP (classic) | rs2099902 |
ClinGen | rs2099902 |
ebi | rs2099902 |
HLI | rs2099902 |
Exac | rs2099902 |
Gnomad | rs2099902 |
Varsome | rs2099902 |
LitVar | rs2099902 |
Map | rs2099902 |
PheGenI | rs2099902 |
Biobank | rs2099902 |
1000 genomes | rs2099902 |
hgdp | rs2099902 |
ensembl | rs2099902 |
geneview | rs2099902 |
scholar | rs2099902 |
rs2099902 | |
pharmgkb | rs2099902 |
gwascentral | rs2099902 |
openSNP | rs2099902 |
23andMe | rs2099902 |
SNPshot | rs2099902 |
SNPdbe | rs2099902 |
MSV3d | rs2099902 |
GWAS Ctlg | rs2099902 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
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[PMID 30482481] SNPs in 3'-UTR region of MBL2 increases susceptibility to recurrent vulvovaginal infections by altering sMBL levels.
[PMID 31141020] Association between MBL2 haplotypes and dengue severity in children from Rio de Janeiro, Brazil.