rs77952980
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs77952980(A;A) |
Make rs77952980(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 22 |
Position | 42128152 |
Gene | CYP2D6, LOC102723722, LOC107987465, LOC107987481 |
is a | snp |
is | mentioned by |
dbSNP | rs77952980 |
dbSNP (classic) | rs77952980 |
ClinGen | rs77952980 |
ebi | rs77952980 |
HLI | rs77952980 |
Exac | rs77952980 |
Gnomad | rs77952980 |
Varsome | rs77952980 |
LitVar | rs77952980 |
Map | rs77952980 |
PheGenI | rs77952980 |
Biobank | rs77952980 |
1000 genomes | rs77952980 |
hgdp | rs77952980 |
ensembl | rs77952980 |
geneview | rs77952980 |
scholar | rs77952980 |
rs77952980 | |
pharmgkb | rs77952980 |
gwascentral | rs77952980 |
openSNP | rs77952980 |
23andMe | rs77952980 |
SNPshot | rs77952980 |
SNPdbe | rs77952980 |
MSV3d | rs77952980 |
GWAS Ctlg | rs77952980 |
Max Magnitude | 0 |
a variation in CYP2D6