rs17076812
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs17076812(A;G) |
Make rs17076812(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 6421917 |
Gene | MCPH1 |
is a | snp |
is | mentioned by |
dbSNP | rs17076812 |
dbSNP (classic) | rs17076812 |
ClinGen | rs17076812 |
ebi | rs17076812 |
HLI | rs17076812 |
Exac | rs17076812 |
Gnomad | rs17076812 |
Varsome | rs17076812 |
LitVar | rs17076812 |
Map | rs17076812 |
PheGenI | rs17076812 |
Biobank | rs17076812 |
1000 genomes | rs17076812 |
hgdp | rs17076812 |
ensembl | rs17076812 |
geneview | rs17076812 |
scholar | rs17076812 |
rs17076812 | |
pharmgkb | rs17076812 |
gwascentral | rs17076812 |
openSNP | rs17076812 |
23andMe | rs17076812 |
SNPshot | rs17076812 |
SNPdbe | rs17076812 |
MSV3d | rs17076812 |
GWAS Ctlg | rs17076812 |
GMAF | 0.1212 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19028548] mentioned as potentially affecting grey matter volume, sample size tiny