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rs387906867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906867(G;T)
Make rs387906867(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position44942489
GeneSIX3, SIX3-AS1
is asnp
is mentioned by
dbSNPrs387906867
ebirs387906867
HLIrs387906867
Exacrs387906867
Varsomers387906867
Maprs387906867
PheGenIrs387906867
hapmaprs387906867
1000 genomesrs387906867
hgdprs387906867
ensemblrs387906867
gopubmedrs387906867
geneviewrs387906867
scholarrs387906867
googlers387906867
pharmgkbrs387906867
gwascentralrs387906867
openSNPrs387906867
23andMers387906867
23andMe allrs387906867
SNP Nexus

SNPshotrs387906867
SNPdbers387906867
MSV3drs387906867
GWAS Ctlgrs387906867
Max Magnitude0
ClinVar
Risk rs387906867(T;T)
Alt rs387906867(T;T)
Reference rs387906867(G;G)
Significance Pathogenic
Disease Holoprosencephaly 2 SCHIZENCEPHALY
Variation info
Gene SIX3 SIX3-AS1
CLNDBN Holoprosencephaly 2 SCHIZENCEPHALY
Reversed 0
HGVS NC_000002.11:g.45169628G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023328.2, RCV000023329.2,