rs1007371
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | |
(T;T) | 1.2 | rare genotype. |
Make rs1007371(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 80326220 |
Gene | CTNNA2, LOC107985904 |
is a | snp |
is | mentioned by |
dbSNP | rs1007371 |
dbSNP (classic) | rs1007371 |
ClinGen | rs1007371 |
ebi | rs1007371 |
HLI | rs1007371 |
Exac | rs1007371 |
Gnomad | rs1007371 |
Varsome | rs1007371 |
LitVar | rs1007371 |
Map | rs1007371 |
PheGenI | rs1007371 |
Biobank | rs1007371 |
1000 genomes | rs1007371 |
hgdp | rs1007371 |
ensembl | rs1007371 |
geneview | rs1007371 |
scholar | rs1007371 |
rs1007371 | |
pharmgkb | rs1007371 |
gwascentral | rs1007371 |
openSNP | rs1007371 |
23andMe | rs1007371 |
SNPshot | rs1007371 |
SNPdbe | rs1007371 |
MSV3d | rs1007371 |
GWAS Ctlg | rs1007371 |
GMAF | 0.2052 |
Max Magnitude | 1.2 |
[PMID 17667961] having minor alleles at all 3 of rs1446109-rs1007371-rs723524 may affect left-right asymmetrical brain function, such as handedness, and much of human cognition, behavior and emotion. pdf full paper