rs149048873
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs149048873(A;A) |
Make rs149048873(A;G) |
Make rs149048873(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 21 |
Position | 34615146 |
Gene | RCAN1 |
is a | snp |
is | mentioned by |
dbSNP | rs149048873 |
dbSNP (classic) | rs149048873 |
ClinGen | rs149048873 |
ebi | rs149048873 |
HLI | rs149048873 |
Exac | rs149048873 |
Gnomad | rs149048873 |
Varsome | rs149048873 |
LitVar | rs149048873 |
Map | rs149048873 |
PheGenI | rs149048873 |
Biobank | rs149048873 |
1000 genomes | rs149048873 |
hgdp | rs149048873 |
ensembl | rs149048873 |
geneview | rs149048873 |
scholar | rs149048873 |
rs149048873 | |
pharmgkb | rs149048873 |
gwascentral | rs149048873 |
openSNP | rs149048873 |
23andMe | rs149048873 |
SNPshot | rs149048873 |
SNPdbe | rs149048873 |
MSV3d | rs149048873 |
GWAS Ctlg | rs149048873 |
Max Magnitude | 0 |
[PMID 25863471] Association Between Sequence Variations in RCAN1 Promoter and the Risk of Sporadic Congenital Heart Disease in a Chinese Population