rs12603112
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12603112(A;A) |
Make rs12603112(A;G) |
Make rs12603112(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 50588988 |
Gene | CACNA1G |
is a | snp |
is | mentioned by |
dbSNP | rs12603112 |
dbSNP (classic) | rs12603112 |
ClinGen | rs12603112 |
ebi | rs12603112 |
HLI | rs12603112 |
Exac | rs12603112 |
Gnomad | rs12603112 |
Varsome | rs12603112 |
LitVar | rs12603112 |
Map | rs12603112 |
PheGenI | rs12603112 |
Biobank | rs12603112 |
1000 genomes | rs12603112 |
hgdp | rs12603112 |
ensembl | rs12603112 |
geneview | rs12603112 |
scholar | rs12603112 |
rs12603112 | |
pharmgkb | rs12603112 |
gwascentral | rs12603112 |
openSNP | rs12603112 |
23andMe | rs12603112 |
SNPshot | rs12603112 |
SNPdbe | rs12603112 |
MSV3d | rs12603112 |
GWAS Ctlg | rs12603112 |
GMAF | 0.4192 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
23andMe blog each copy of an G at rs12603112 increases the odds of autism in boys by 2.2x, although the G is very common