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rs878853251

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853251(-;-)
Make rs878853251(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position142760551
GeneHIVEP2
is asnp
is mentioned by
dbSNPrs878853251
ebirs878853251
HLIrs878853251
Exacrs878853251
Varsomers878853251
Maprs878853251
PheGenIrs878853251
hapmaprs878853251
1000 genomesrs878853251
hgdprs878853251
ensemblrs878853251
gopubmedrs878853251
geneviewrs878853251
scholarrs878853251
googlers878853251
pharmgkbrs878853251
gwascentralrs878853251
openSNPrs878853251
23andMers878853251
23andMe allrs878853251
SNP Nexus

SNPshotrs878853251
SNPdbers878853251
MSV3drs878853251
GWAS Ctlgrs878853251
Max Magnitude0
ClinVar
Risk rs878853251(;)
Alt rs878853251(;)
Reference rs878853251(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene HIVEP2
CLNDBN Mental retardation, autosomal dominant 43
Reversed 1
HGVS NC_000006.11:g.143081688delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000225131.1,