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rs398123008

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123008(C;T)
Make rs398123008(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position56834922
GeneC17orf67, DGKE
is asnp
is mentioned by
dbSNPrs398123008
ebirs398123008
HLIrs398123008
Exacrs398123008
Varsomers398123008
Maprs398123008
PheGenIrs398123008
hapmaprs398123008
1000 genomesrs398123008
hgdprs398123008
ensemblrs398123008
gopubmedrs398123008
geneviewrs398123008
scholarrs398123008
googlers398123008
pharmgkbrs398123008
gwascentralrs398123008
openSNPrs398123008
23andMers398123008
23andMe allrs398123008
SNP Nexus

SNPshotrs398123008
SNPdbers398123008
MSV3drs398123008
GWAS Ctlgrs398123008
Max Magnitude0
ClinVar
Risk rs398123008(T;T)
Alt rs398123008(T;T)
Reference rs398123008(C;C)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene DGKE C17orf67
CLNDBN Nephrotic syndrome, type 7
Reversed 0
HGVS NC_000017.10:g.54912283C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032778.3,