rs2975766
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs2975766(A;A) |
Make rs2975766(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 240598657 |
Gene | CAPN10 |
is a | snp |
is | mentioned by |
dbSNP | rs2975766 |
dbSNP (classic) | rs2975766 |
ClinGen | rs2975766 |
ebi | rs2975766 |
HLI | rs2975766 |
Exac | rs2975766 |
Gnomad | rs2975766 |
Varsome | rs2975766 |
LitVar | rs2975766 |
Map | rs2975766 |
PheGenI | rs2975766 |
Biobank | rs2975766 |
1000 genomes | rs2975766 |
hgdp | rs2975766 |
ensembl | rs2975766 |
geneview | rs2975766 |
scholar | rs2975766 |
rs2975766 | |
pharmgkb | rs2975766 |
gwascentral | rs2975766 |
openSNP | rs2975766 |
23andMe | rs2975766 |
SNPshot | rs2975766 |
SNPdbe | rs2975766 |
MSV3d | rs2975766 |
GWAS Ctlg | rs2975766 |
GMAF | 0.01331 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19416960] Mouse population-guided resequencing reveals that variants in CD44 contribute to acetaminophen-induced liver injury in humans.