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rs869312859

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312859(-;-)
Make rs869312859(-;T)
Make rs869312859(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7204200
GeneDLG4
is asnp
is mentioned by
dbSNPrs869312859
ebirs869312859
HLIrs869312859
Exacrs869312859
Varsomers869312859
Maprs869312859
PheGenIrs869312859
hapmaprs869312859
1000 genomesrs869312859
hgdprs869312859
ensemblrs869312859
gopubmedrs869312859
geneviewrs869312859
scholarrs869312859
googlers869312859
pharmgkbrs869312859
gwascentralrs869312859
openSNPrs869312859
23andMers869312859
23andMe allrs869312859
SNP Nexus

SNPshotrs869312859
SNPdbers869312859
MSV3drs869312859
GWAS Ctlgrs869312859
Max Magnitude0
ClinVar
Risk rs869312859(T;T)
Alt rs869312859(T;T)
Reference rs869312859(;)
Significance Probable-Pathogenic
Disease Cerebral visual impairment and intellectual disability
Variation info
Gene DLG4
CLNDBN Cerebral visual impairment and intellectual disability
Reversed 1
HGVS NC_000017.10:g.7107520dupA
CLNSRC
CLNACC RCV000210399.1,