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rs312262698

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs312262698(-;T)
Make rs312262698(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position56844026
GeneDGKE
is asnp
is mentioned by
dbSNPrs312262698
ClinGenrs312262698
ebirs312262698
HLIrs312262698
Exacrs312262698
Varsomers312262698
Maprs312262698
PheGenIrs312262698
hapmaprs312262698
1000 genomesrs312262698
hgdprs312262698
ensemblrs312262698
gopubmedrs312262698
geneviewrs312262698
scholarrs312262698
googlers312262698
pharmgkbrs312262698
gwascentralrs312262698
openSNPrs312262698
23andMers312262698
23andMe allrs312262698
SNP Nexus

SNPshotrs312262698
SNPdbers312262698
MSV3drs312262698
GWAS Ctlgrs312262698
Max Magnitude0
ClinVar
Risk rs312262698(T;T)
Alt rs312262698(T;T)
Reference Rs312262698(;)
Significance Probable-Pathogenic
Disease Atypical hemolytic uremic syndrome
Variation info
Gene DGKE
CLNDBN Atypical hemolytic uremic syndrome
Reversed 0
HGVS NC_000017.10:g.54921387dupT
CLNSRC ClinVar
CLNACC RCV000122613.1,