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rs878853142

From SNPedia

Orientationplus
Geno Mag Summary
(ATGGC;ATGGC) 0 common in clinvar
Make rs878853142(-;-)
Make rs878853142(-;GGCAT)
Make rs878853142(GGCAT;GGCAT)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17795280
GeneRAI1
is asnp
is mentioned by
dbSNPrs878853142
ebirs878853142
HLIrs878853142
Exacrs878853142
Varsomers878853142
Maprs878853142
PheGenIrs878853142
hapmaprs878853142
1000 genomesrs878853142
hgdprs878853142
ensemblrs878853142
gopubmedrs878853142
geneviewrs878853142
scholarrs878853142
googlers878853142
pharmgkbrs878853142
gwascentralrs878853142
openSNPrs878853142
23andMers878853142
23andMe allrs878853142
SNP Nexus

SNPshotrs878853142
SNPdbers878853142
MSV3drs878853142
GWAS Ctlgrs878853142
Max Magnitude0
ClinVar
Risk rs878853142(;)
Alt rs878853142(;)
Reference rs878853142(ATGGC;ATGGC)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene RAI1
CLNDBN Intellectual disability
Reversed 0
HGVS NC_000017.10:g.17698594_17698598delGGCAT
CLNSRC
CLNACC RCV000224248.1,