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rs878853141

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853141(C;C)
Make rs878853141(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position53199068
GeneKDM5C, MIR6894
is asnp
is mentioned by
dbSNPrs878853141
ebirs878853141
HLIrs878853141
Exacrs878853141
Varsomers878853141
Maprs878853141
PheGenIrs878853141
hapmaprs878853141
1000 genomesrs878853141
hgdprs878853141
ensemblrs878853141
gopubmedrs878853141
geneviewrs878853141
scholarrs878853141
googlers878853141
pharmgkbrs878853141
gwascentralrs878853141
openSNPrs878853141
23andMers878853141
23andMe allrs878853141
SNP Nexus

SNPshotrs878853141
SNPdbers878853141
MSV3drs878853141
GWAS Ctlgrs878853141
Max Magnitude0
ClinVar
Risk rs878853141(C;C)
Alt rs878853141(C;C)
Reference rs878853141(G;G)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene MIR6894 KDM5C
CLNDBN Intellectual disability
Reversed 1
HGVS NC_000023.10:g.53228250C>G
CLNSRC
CLNACC RCV000224884.1,