rs2286149
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2286149(C;C) |
Make rs2286149(C;T) |
Make rs2286149(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 106659346 |
Gene | CCDC71L, CTB-30L5.1 |
is a | snp |
is | mentioned by |
dbSNP | rs2286149 |
dbSNP (classic) | rs2286149 |
ClinGen | rs2286149 |
ebi | rs2286149 |
HLI | rs2286149 |
Exac | rs2286149 |
Gnomad | rs2286149 |
Varsome | rs2286149 |
LitVar | rs2286149 |
Map | rs2286149 |
PheGenI | rs2286149 |
Biobank | rs2286149 |
1000 genomes | rs2286149 |
hgdp | rs2286149 |
ensembl | rs2286149 |
geneview | rs2286149 |
scholar | rs2286149 |
rs2286149 | |
pharmgkb | rs2286149 |
gwascentral | rs2286149 |
openSNP | rs2286149 |
23andMe | rs2286149 |
SNPshot | rs2286149 |
SNPdbe | rs2286149 |
MSV3d | rs2286149 |
GWAS Ctlg | rs2286149 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24951662] Sequencing of 2 Subclinical Atherosclerosis Candidate Regions in 3669 Individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study