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

rs878853269

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853269(C;T)
Make rs878853269(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position142771183
GeneHIVEP2
is asnp
is mentioned by
dbSNPrs878853269
ebirs878853269
HLIrs878853269
Exacrs878853269
Varsomers878853269
Maprs878853269
PheGenIrs878853269
hapmaprs878853269
1000 genomesrs878853269
hgdprs878853269
ensemblrs878853269
gopubmedrs878853269
geneviewrs878853269
scholarrs878853269
googlers878853269
pharmgkbrs878853269
gwascentralrs878853269
openSNPrs878853269
23andMers878853269
23andMe allrs878853269
SNP Nexus

SNPshotrs878853269
SNPdbers878853269
MSV3drs878853269
GWAS Ctlgrs878853269
Max Magnitude0
ClinVar
Risk rs878853269(T;T)
Alt rs878853269(T;T)
Reference rs878853269(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene HIVEP2
CLNDBN Mental retardation, autosomal dominant 43
Reversed 1
HGVS NC_000006.11:g.143092320G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000225329.1,