rs2266879
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2266879(A;A) |
Make rs2266879(A;G) |
Make rs2266879(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 153770343 |
Gene | PLXNB3 |
is a | snp |
is | mentioned by |
dbSNP | rs2266879 |
dbSNP (classic) | rs2266879 |
ClinGen | rs2266879 |
ebi | rs2266879 |
HLI | rs2266879 |
Exac | rs2266879 |
Gnomad | rs2266879 |
Varsome | rs2266879 |
LitVar | rs2266879 |
Map | rs2266879 |
PheGenI | rs2266879 |
Biobank | rs2266879 |
1000 genomes | rs2266879 |
hgdp | rs2266879 |
ensembl | rs2266879 |
geneview | rs2266879 |
scholar | rs2266879 |
rs2266879 | |
pharmgkb | rs2266879 |
gwascentral | rs2266879 |
openSNP | rs2266879 |
23andMe | rs2266879 |
SNPshot | rs2266879 |
SNPdbe | rs2266879 |
MSV3d | rs2266879 |
GWAS Ctlg | rs2266879 |
GMAF | 0.3676 |
Max Magnitude | 0 |
[PMID 17033634] - relevant to a human-specific 'haplotype A' in PLXNB3, along with E1156D (rs6643791), and V1596E. HapA carriers showed higher vocabulary performance scores and increased white matter volume, in comparison to non-carriers.