rs140198372
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs140198372(A;A) |
Make rs140198372(A;C) |
Make rs140198372(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 14 |
Position | 94487495 |
Gene | SERPINA12 |
is a | snp |
is | mentioned by |
dbSNP | rs140198372 |
dbSNP (classic) | rs140198372 |
ClinGen | rs140198372 |
ebi | rs140198372 |
HLI | rs140198372 |
Exac | rs140198372 |
Gnomad | rs140198372 |
Varsome | rs140198372 |
LitVar | rs140198372 |
Map | rs140198372 |
PheGenI | rs140198372 |
Biobank | rs140198372 |
1000 genomes | rs140198372 |
hgdp | rs140198372 |
ensembl | rs140198372 |
geneview | rs140198372 |
scholar | rs140198372 |
rs140198372 | |
pharmgkb | rs140198372 |
gwascentral | rs140198372 |
openSNP | rs140198372 |
23andMe | rs140198372 |
SNPshot | rs140198372 |
SNPdbe | rs140198372 |
MSV3d | rs140198372 |
GWAS Ctlg | rs140198372 |
Max Magnitude | 0 |
[PMID 26917578] Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.