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rs878853151

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853151(-;-)
Make rs878853151(-;T)
Make rs878853151(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position53211601
GeneKDM5C
is asnp
is mentioned by
dbSNPrs878853151
ebirs878853151
HLIrs878853151
Exacrs878853151
Varsomers878853151
Maprs878853151
PheGenIrs878853151
hapmaprs878853151
1000 genomesrs878853151
hgdprs878853151
ensemblrs878853151
gopubmedrs878853151
geneviewrs878853151
scholarrs878853151
googlers878853151
pharmgkbrs878853151
gwascentralrs878853151
openSNPrs878853151
23andMers878853151
23andMe allrs878853151
SNP Nexus

SNPshotrs878853151
SNPdbers878853151
MSV3drs878853151
GWAS Ctlgrs878853151
Max Magnitude0
ClinVar
Risk rs878853151(T;T)
Alt rs878853151(T;T)
Reference rs878853151(;)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene KDM5C
CLNDBN Intellectual disability
Reversed 1
HGVS NC_000023.10:g.53240784dupA
CLNSRC
CLNACC RCV000224502.1,