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rs397514667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514667(A;A)
Make rs397514667(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position6445445
GeneCD27
is asnp
is mentioned by
dbSNPrs397514667
ebirs397514667
HLIrs397514667
Exacrs397514667
Varsomers397514667
Maprs397514667
PheGenIrs397514667
hapmaprs397514667
1000 genomesrs397514667
hgdprs397514667
ensemblrs397514667
gopubmedrs397514667
geneviewrs397514667
scholarrs397514667
googlers397514667
pharmgkbrs397514667
gwascentralrs397514667
openSNPrs397514667
23andMers397514667
23andMe allrs397514667
SNP Nexus

SNPshotrs397514667
SNPdbers397514667
MSV3drs397514667
GWAS Ctlgrs397514667
Max Magnitude0
ClinVar
Risk rs397514667(A;A)
Alt rs397514667(A;A)
Reference rs397514667(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.6554611G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033860.25,