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rs138228629

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138228629(A;A)
Make rs138228629(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome13
Position24906342
GeneCENPJ
is asnp
is mentioned by
dbSNPrs138228629
dbSNP (classic)rs138228629
ClinGenrs138228629
ebirs138228629
HLIrs138228629
Exacrs138228629
Gnomadrs138228629
Varsomers138228629
LitVarrs138228629
Maprs138228629
PheGenIrs138228629
Biobankrs138228629
1000 genomesrs138228629
hgdprs138228629
ensemblrs138228629
geneviewrs138228629
scholarrs138228629
googlers138228629
pharmgkbrs138228629
gwascentralrs138228629
openSNPrs138228629
23andMers138228629
SNPshotrs138228629
SNPdbers138228629
MSV3drs138228629
GWAS Ctlgrs138228629
Max Magnitude0
ClinVar
Risk rs138228629(A;A)
Alt rs138228629(A;A)
Reference Rs138228629(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CENPJ
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.25480480G>A
CLNSRC
CLNACC RCV000369854.1,