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

rs864309676

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864309676(A;C)
Make rs864309676(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position132472372
GeneSTX7
is asnp
is mentioned by
dbSNPrs864309676
ebirs864309676
HLIrs864309676
Exacrs864309676
Varsomers864309676
Maprs864309676
PheGenIrs864309676
hapmaprs864309676
1000 genomesrs864309676
hgdprs864309676
ensemblrs864309676
gopubmedrs864309676
geneviewrs864309676
scholarrs864309676
googlers864309676
pharmgkbrs864309676
gwascentralrs864309676
openSNPrs864309676
23andMers864309676
23andMe allrs864309676
SNP Nexus

SNPshotrs864309676
SNPdbers864309676
MSV3drs864309676
GWAS Ctlgrs864309676
Max Magnitude0
ClinVar
Risk rs864309676(C;C)
Alt rs864309676(C;C)
Reference rs864309676(A;A)
Significance Probable-Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene STX7
CLNDBN Abnormality of neuronal migration
Reversed 1
HGVS NC_000006.11:g.132793511T>G
CLNSRC
CLNACC RCV000203258.1,