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rs398122958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122958(A;A)
Make rs398122958(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position53186696
GenePRKCD
is asnp
is mentioned by
dbSNPrs398122958
ebirs398122958
HLIrs398122958
Exacrs398122958
Varsomers398122958
Maprs398122958
PheGenIrs398122958
hapmaprs398122958
1000 genomesrs398122958
hgdprs398122958
ensemblrs398122958
gopubmedrs398122958
geneviewrs398122958
scholarrs398122958
googlers398122958
pharmgkbrs398122958
gwascentralrs398122958
openSNPrs398122958
23andMers398122958
23andMe allrs398122958
SNP Nexus

SNPshotrs398122958
SNPdbers398122958
MSV3drs398122958
GWAS Ctlgrs398122958
Max Magnitude0
ClinVar
Risk rs398122958(A;A)
Alt rs398122958(A;A)
Reference rs398122958(G;G)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene PRKCD
CLNDBN Autoimmune lymphoproliferative syndrome, type III
Reversed 0
HGVS NC_000003.11:g.53220712G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074607.10,