rs3769048
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs3769048(C;T) |
Make rs3769048(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 237861218 |
Gene | RAMP1 |
is a | snp |
is | mentioned by |
dbSNP | rs3769048 |
dbSNP (classic) | rs3769048 |
ClinGen | rs3769048 |
ebi | rs3769048 |
HLI | rs3769048 |
Exac | rs3769048 |
Gnomad | rs3769048 |
Varsome | rs3769048 |
LitVar | rs3769048 |
Map | rs3769048 |
PheGenI | rs3769048 |
Biobank | rs3769048 |
1000 genomes | rs3769048 |
hgdp | rs3769048 |
ensembl | rs3769048 |
geneview | rs3769048 |
scholar | rs3769048 |
rs3769048 | |
pharmgkb | rs3769048 |
gwascentral | rs3769048 |
openSNP | rs3769048 |
23andMe | rs3769048 |
SNPshot | rs3769048 |
SNPdbe | rs3769048 |
MSV3d | rs3769048 |
GWAS Ctlg | rs3769048 |
GMAF | 0.07759 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19710695] Haplotype-based case-control study of receptor (calcitonin) activity-modifying protein-1 gene in cerebral infarction