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

rs387906868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906868(G;T)
Make rs387906868(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position44942603
GeneSIX3, SIX3-AS1
is asnp
is mentioned by
dbSNPrs387906868
ebirs387906868
HLIrs387906868
Exacrs387906868
Varsomers387906868
Maprs387906868
PheGenIrs387906868
hapmaprs387906868
1000 genomesrs387906868
hgdprs387906868
ensemblrs387906868
gopubmedrs387906868
geneviewrs387906868
scholarrs387906868
googlers387906868
pharmgkbrs387906868
gwascentralrs387906868
openSNPrs387906868
23andMers387906868
23andMe allrs387906868
SNP Nexus

SNPshotrs387906868
SNPdbers387906868
MSV3drs387906868
GWAS Ctlgrs387906868
Max Magnitude0
ClinVar
Risk rs387906868(T;T)
Alt rs387906868(T;T)
Reference rs387906868(G;G)
Significance Pathogenic
Disease SCHIZENCEPHALY
Variation info
Gene SIX3 SIX3-AS1
CLNDBN SCHIZENCEPHALY
Reversed 0
HGVS NC_000002.11:g.45169742G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023332.2,