rs7557078
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7557078(A;A) |
Make rs7557078(A;C) |
Make rs7557078(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 237881216 |
Gene | RAMP1 |
is a | snp |
is | mentioned by |
dbSNP | rs7557078 |
dbSNP (classic) | rs7557078 |
ClinGen | rs7557078 |
ebi | rs7557078 |
HLI | rs7557078 |
Exac | rs7557078 |
Gnomad | rs7557078 |
Varsome | rs7557078 |
LitVar | rs7557078 |
Map | rs7557078 |
PheGenI | rs7557078 |
Biobank | rs7557078 |
1000 genomes | rs7557078 |
hgdp | rs7557078 |
ensembl | rs7557078 |
geneview | rs7557078 |
scholar | rs7557078 |
rs7557078 | |
pharmgkb | rs7557078 |
gwascentral | rs7557078 |
openSNP | rs7557078 |
23andMe | rs7557078 |
SNPshot | rs7557078 |
SNPdbe | rs7557078 |
MSV3d | rs7557078 |
GWAS Ctlg | rs7557078 |
GMAF | 0.2374 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19710695] Haplotype-based case-control study of receptor (calcitonin) activity-modifying protein-1 gene in cerebral infarction