rs10199956
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10199956(G;G) |
Make rs10199956(G;T) |
Make rs10199956(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 237907946 |
Gene | RAMP1 |
is a | snp |
is | mentioned by |
dbSNP | rs10199956 |
dbSNP (classic) | rs10199956 |
ClinGen | rs10199956 |
ebi | rs10199956 |
HLI | rs10199956 |
Exac | rs10199956 |
Gnomad | rs10199956 |
Varsome | rs10199956 |
LitVar | rs10199956 |
Map | rs10199956 |
PheGenI | rs10199956 |
Biobank | rs10199956 |
1000 genomes | rs10199956 |
hgdp | rs10199956 |
ensembl | rs10199956 |
geneview | rs10199956 |
scholar | rs10199956 |
rs10199956 | |
pharmgkb | rs10199956 |
gwascentral | rs10199956 |
openSNP | rs10199956 |
23andMe | rs10199956 |
SNPshot | rs10199956 |
SNPdbe | rs10199956 |
MSV3d | rs10199956 |
GWAS Ctlg | rs10199956 |
GMAF | 0.4426 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
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[PMID 19710695] Haplotype-based case-control study of receptor (calcitonin) activity-modifying protein-1 gene in cerebral infarction