rs10772266
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10772266(A;A) |
Make rs10772266(A;G) |
Make rs10772266(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 10353570 |
Gene | KLRD1 |
is a | snp |
is | mentioned by |
dbSNP | rs10772266 |
dbSNP (classic) | rs10772266 |
ClinGen | rs10772266 |
ebi | rs10772266 |
HLI | rs10772266 |
Exac | rs10772266 |
Gnomad | rs10772266 |
Varsome | rs10772266 |
LitVar | rs10772266 |
Map | rs10772266 |
PheGenI | rs10772266 |
Biobank | rs10772266 |
1000 genomes | rs10772266 |
hgdp | rs10772266 |
ensembl | rs10772266 |
geneview | rs10772266 |
scholar | rs10772266 |
rs10772266 | |
pharmgkb | rs10772266 |
gwascentral | rs10772266 |
openSNP | rs10772266 |
23andMe | rs10772266 |
SNPshot | rs10772266 |
SNPdbe | rs10772266 |
MSV3d | rs10772266 |
GWAS Ctlg | rs10772266 |
GMAF | 0.4091 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20587610] Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection