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rs398122933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122933(A;A)
Make rs398122933(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position6445119
GeneCD27
is asnp
is mentioned by
dbSNPrs398122933
ebirs398122933
HLIrs398122933
Exacrs398122933
Varsomers398122933
Maprs398122933
PheGenIrs398122933
hapmaprs398122933
1000 genomesrs398122933
hgdprs398122933
ensemblrs398122933
gopubmedrs398122933
geneviewrs398122933
scholarrs398122933
googlers398122933
pharmgkbrs398122933
gwascentralrs398122933
openSNPrs398122933
23andMers398122933
23andMe allrs398122933
SNP Nexus

SNPshotrs398122933
SNPdbers398122933
MSV3drs398122933
GWAS Ctlgrs398122933
Max Magnitude0
ClinVar
Risk rs398122933(A;A)
Alt rs398122933(A;A)
Reference Rs398122933(G;G)
Significance Pathogenic
Disease Lymphoproliferative syndrome 2
Variation info
Gene CD27-AS1 CD27
CLNDBN Lymphoproliferative syndrome 2
Reversed 0
HGVS NC_000012.11:g.6554285G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033859.25,