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rs863224877

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224877(A;G)
Make rs863224877(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position72351840
GeneHDAC8
is asnp
is mentioned by
dbSNPrs863224877
ebirs863224877
HLIrs863224877
Exacrs863224877
Varsomers863224877
Maprs863224877
PheGenIrs863224877
hapmaprs863224877
1000 genomesrs863224877
hgdprs863224877
ensemblrs863224877
gopubmedrs863224877
geneviewrs863224877
scholarrs863224877
googlers863224877
pharmgkbrs863224877
gwascentralrs863224877
openSNPrs863224877
23andMers863224877
23andMe allrs863224877
SNP Nexus

SNPshotrs863224877
SNPdbers863224877
MSV3drs863224877
GWAS Ctlgrs863224877
Max Magnitude0
ClinVar
Risk rs863224877(G;G)
Alt rs863224877(G;G)
Reference rs863224877(A;A)
Significance Probable-Pathogenic
Disease Cornelia de Lange syndrome 5
Variation info
Gene HDAC8
CLNDBN Cornelia de Lange syndrome 5
Reversed 1
HGVS NC_000023.10:g.71571690T>C
CLNSRC
CLNACC RCV000196804.1,