Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060499708

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499708(A;A)
Make rs1060499708(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position56861882
GeneDGKE
is asnp
is mentioned by
dbSNPrs1060499708
dbSNP (old)rs1060499708
ClinGenrs1060499708
ebirs1060499708
HLIrs1060499708
Exacrs1060499708
Gnomadrs1060499708
Varsomers1060499708
Maprs1060499708
PheGenIrs1060499708
Biobankrs1060499708
1000 genomesrs1060499708
hgdprs1060499708
ensemblrs1060499708
gopubmedrs1060499708
geneviewrs1060499708
scholarrs1060499708
googlers1060499708
pharmgkbrs1060499708
gwascentralrs1060499708
openSNPrs1060499708
23andMers1060499708
23andMe allrs1060499708
SNPshotrs1060499708
SNPdbers1060499708
MSV3drs1060499708
GWAS Ctlgrs1060499708
Max Magnitude0
ClinVar
Risk rs1060499708(A;A)
Alt rs1060499708(A;A)
Reference Rs1060499708(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene DGKE
CLNDBN Nephrotic syndrome, type 7
Reversed 0
HGVS NC_000017.10:g.54939243G>A
CLNSRC
CLNACC RCV000449567.1,