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rs6639946

From SNPedia

Orientationplus
Stabilizedplus
Make rs6639946(C;C)
Make rs6639946(C;G)
Make rs6639946(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position7843604
GeneVCX
is asnp
is mentioned by
dbSNPrs6639946
ebirs6639946
HLIrs6639946
Exacrs6639946
Varsomers6639946
Maprs6639946
PheGenIrs6639946
hapmaprs6639946
1000 genomesrs6639946
hgdprs6639946
ensemblrs6639946
gopubmedrs6639946
geneviewrs6639946
scholarrs6639946
googlers6639946
pharmgkbrs6639946
gwascentralrs6639946
openSNPrs6639946
23andMers6639946
23andMe allrs6639946
SNP Nexus

SNPshotrs6639946
SNPdbers6639946
MSV3drs6639946
GWAS Ctlgrs6639946
Max Magnitude
Venter snp
Source plos
Gene VCX
allele G
frequency
sift TOLERATED
HuRef 1103673004407
Disease Association Defects in VCX3A are associated with some forms of X- linked nonspecific mental retardation.