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rs1060499709

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499709(A;A)
Make rs1060499709(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position56856582
GeneDGKE
is asnp
is mentioned by
dbSNPrs1060499709
dbSNP (old)rs1060499709
ClinGenrs1060499709
ebirs1060499709
HLIrs1060499709
Exacrs1060499709
Gnomadrs1060499709
Varsomers1060499709
Maprs1060499709
PheGenIrs1060499709
Biobankrs1060499709
1000 genomesrs1060499709
hgdprs1060499709
ensemblrs1060499709
gopubmedrs1060499709
geneviewrs1060499709
scholarrs1060499709
googlers1060499709
pharmgkbrs1060499709
gwascentralrs1060499709
openSNPrs1060499709
23andMers1060499709
23andMe allrs1060499709
SNP Nexus

SNPshotrs1060499709
SNPdbers1060499709
MSV3drs1060499709
GWAS Ctlgrs1060499709
Max Magnitude0
ClinVar
Risk rs1060499709(A;A)
Alt rs1060499709(A;A)
Reference Rs1060499709(G;G)
Significance Probable-Pathogenic
Disease Nephrotic syndrome
Variation info
Gene DGKE
CLNDBN Nephrotic syndrome, type 7
Reversed 0
HGVS NC_000017.10:g.54933943G>A
CLNSRC
CLNACC RCV000449615.1,