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rs864321658

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321658(C;C)
Make rs864321658(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position24885671
GeneCENPJ, RNF17
is asnp
is mentioned by
dbSNPrs864321658
ebirs864321658
HLIrs864321658
Exacrs864321658
Varsomers864321658
Maprs864321658
PheGenIrs864321658
hapmaprs864321658
1000 genomesrs864321658
hgdprs864321658
ensemblrs864321658
gopubmedrs864321658
geneviewrs864321658
scholarrs864321658
googlers864321658
pharmgkbrs864321658
gwascentralrs864321658
openSNPrs864321658
23andMers864321658
23andMe allrs864321658
SNP Nexus

SNPshotrs864321658
SNPdbers864321658
MSV3drs864321658
GWAS Ctlgrs864321658
Max Magnitude0
ClinVar
Risk rs864321658(C;C)
Alt rs864321658(C;C)
Reference rs864321658(G;G)
Significance Pathogenic
Disease Seckel syndrome 4
Variation info
Gene CENPJ
CLNDBN Seckel syndrome 4
Reversed 1
HGVS NC_000013.10:g.25459809C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001893.2,