rs6643791
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6643791(C;C) |
Make rs6643791(C;G) |
Make rs6643791(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 153774047 |
Gene | PLXNB3 |
is a | snp |
is | mentioned by |
dbSNP | rs6643791 |
dbSNP (classic) | rs6643791 |
ClinGen | rs6643791 |
ebi | rs6643791 |
HLI | rs6643791 |
Exac | rs6643791 |
Gnomad | rs6643791 |
Varsome | rs6643791 |
LitVar | rs6643791 |
Map | rs6643791 |
PheGenI | rs6643791 |
Biobank | rs6643791 |
1000 genomes | rs6643791 |
hgdp | rs6643791 |
ensembl | rs6643791 |
geneview | rs6643791 |
scholar | rs6643791 |
rs6643791 | |
pharmgkb | rs6643791 |
gwascentral | rs6643791 |
openSNP | rs6643791 |
23andMe | rs6643791 |
SNPshot | rs6643791 |
SNPdbe | rs6643791 |
MSV3d | rs6643791 |
GWAS Ctlg | rs6643791 |
GMAF | 0.2189 |
Max Magnitude | 0 |
[PMID 17033634] - relevant to a human-specific 'haplotype A' in PLXNB3, along with V598I (rs2266879), and V1596E. HapA carriers showed higher vocabulary performance scores and increased white matter volume, in comparison to non-carriers.