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rs606231297

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231297(C;T)
Make rs606231297(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position53189969
GenePRKCD
is asnp
is mentioned by
dbSNPrs606231297
ebirs606231297
HLIrs606231297
Exacrs606231297
Varsomers606231297
Maprs606231297
PheGenIrs606231297
hapmaprs606231297
1000 genomesrs606231297
hgdprs606231297
ensemblrs606231297
gopubmedrs606231297
geneviewrs606231297
scholarrs606231297
googlers606231297
pharmgkbrs606231297
gwascentralrs606231297
openSNPrs606231297
23andMers606231297
23andMe allrs606231297
SNP Nexus

SNPshotrs606231297
SNPdbers606231297
MSV3drs606231297
GWAS Ctlgrs606231297
Max Magnitude0
ClinVar
Risk rs606231297(T;T)
Alt rs606231297(T;T)
Reference rs606231297(C;C)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene PRKCD
CLNDBN Autoimmune lymphoproliferative syndrome, type III
Reversed 0
HGVS NC_000003.11:g.53223985C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144966.3,