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rs878853146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTTTGGGAA;AGTTTGGGAA) 0 common in clinvar
Make rs878853146(-;-)
Make rs878853146(-;TTGGGAAAGT)
Make rs878853146(TTGGGAAAGT;TTGGGAAAGT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position29917579
GeneIL1RAPL1
is asnp
is mentioned by
dbSNPrs878853146
dbSNP (old)rs878853146
ClinGenrs878853146
ebirs878853146
HLIrs878853146
Exacrs878853146
Varsomers878853146
Maprs878853146
PheGenIrs878853146
Biobankrs878853146
1000 genomesrs878853146
hgdprs878853146
ensemblrs878853146
gopubmedrs878853146
geneviewrs878853146
scholarrs878853146
googlers878853146
pharmgkbrs878853146
gwascentralrs878853146
openSNPrs878853146
23andMers878853146
23andMe allrs878853146
SNP Nexus

SNPshotrs878853146
SNPdbers878853146
MSV3drs878853146
GWAS Ctlgrs878853146
Max Magnitude0
ClinVar
Risk rs878853146(-;-)
Alt rs878853146(-;-)
Reference Rs878853146(AGTTTGGGAA;AGTTTGGGAA)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene IL1RAPL1
CLNDBN Intellectual disability
Reversed 0
HGVS NC_000023.10:g.29935696_29935705delTTGGGAAAGT
CLNSRC
CLNACC RCV000224084.1,