Have questions? Visit https://www.reddit.com/r/SNPedia

rs2266879

From SNPedia

Orientationplus
Stabilizedplus
Make rs2266879(A;A)
Make rs2266879(A;G)
Make rs2266879(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153770343
GenePLXNB3
is asnp
is mentioned by
dbSNPrs2266879
ebirs2266879
HLIrs2266879
Exacrs2266879
Varsomers2266879
Maprs2266879
PheGenIrs2266879
hapmaprs2266879
1000 genomesrs2266879
hgdprs2266879
ensemblrs2266879
gopubmedrs2266879
geneviewrs2266879
scholarrs2266879
googlers2266879
pharmgkbrs2266879
gwascentralrs2266879
openSNPrs2266879
23andMers2266879
23andMe allrs2266879
SNP Nexus

SNPshotrs2266879
SNPdbers2266879
MSV3drs2266879
GWAS Ctlgrs2266879
GMAF0.3676
Max Magnitude
[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.


GET Evidence
PLXNB3-V621I
aa_change Val621Ile
aa_change_short V621I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.506231
summary