rs219778
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs219778(C;C) |
Make rs219778(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 21 |
Position | 36462343 |
Gene | CLDN14, LOC105369301 |
is a | snp |
is | mentioned by |
dbSNP | rs219778 |
dbSNP (classic) | rs219778 |
ClinGen | rs219778 |
ebi | rs219778 |
HLI | rs219778 |
Exac | rs219778 |
Gnomad | rs219778 |
Varsome | rs219778 |
LitVar | rs219778 |
Map | rs219778 |
PheGenI | rs219778 |
Biobank | rs219778 |
1000 genomes | rs219778 |
hgdp | rs219778 |
ensembl | rs219778 |
geneview | rs219778 |
scholar | rs219778 |
rs219778 | |
pharmgkb | rs219778 |
gwascentral | rs219778 |
openSNP | rs219778 |
23andMe | rs219778 |
SNPshot | rs219778 |
SNPdbe | rs219778 |
MSV3d | rs219778 |
GWAS Ctlg | rs219778 |
GMAF | 0.253 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
DeCode reports that carriers of two T alleles at rs219778 have a slightly increased risk of developing kidney stones. [PMID 19561606]