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rs606231296

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231296(A;A)
Make rs606231296(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position53188832
GenePRKCD
is asnp
is mentioned by
dbSNPrs606231296
ebirs606231296
HLIrs606231296
Exacrs606231296
Varsomers606231296
Maprs606231296
PheGenIrs606231296
hapmaprs606231296
1000 genomesrs606231296
hgdprs606231296
ensemblrs606231296
gopubmedrs606231296
geneviewrs606231296
scholarrs606231296
googlers606231296
pharmgkbrs606231296
gwascentralrs606231296
openSNPrs606231296
23andMers606231296
23andMe allrs606231296
SNP Nexus

SNPshotrs606231296
SNPdbers606231296
MSV3drs606231296
GWAS Ctlgrs606231296
Max Magnitude0
ClinVar
Risk rs606231296(A;A)
Alt rs606231296(A;A)
Reference rs606231296(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.53222848G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144965.3,