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rs6643791

From SNPedia

Orientationplus
Stabilizedplus
Make rs6643791(C;C)
Make rs6643791(C;G)
Make rs6643791(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153774047
GenePLXNB3
is asnp
is mentioned by
dbSNPrs6643791
ebirs6643791
HLIrs6643791
Exacrs6643791
Varsomers6643791
Maprs6643791
PheGenIrs6643791
hapmaprs6643791
1000 genomesrs6643791
hgdprs6643791
ensemblrs6643791
gopubmedrs6643791
geneviewrs6643791
scholarrs6643791
googlers6643791
pharmgkbrs6643791
gwascentralrs6643791
openSNPrs6643791
23andMers6643791
23andMe allrs6643791
SNP Nexus

SNPshotrs6643791
SNPdbers6643791
MSV3drs6643791
GWAS Ctlgrs6643791
GMAF0.2189
Max Magnitude
[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.
GET Evidence
PLXNB3-E1179D
aa_change Glu1179Asp
aa_change_short E1179D
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.751881
summary