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rs312262696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs312262696(A;A)
Make rs312262696(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position56848695
GeneDGKE
is asnp
is mentioned by
dbSNPrs312262696
ebirs312262696
HLIrs312262696
Exacrs312262696
Varsomers312262696
Maprs312262696
PheGenIrs312262696
hapmaprs312262696
1000 genomesrs312262696
hgdprs312262696
ensemblrs312262696
gopubmedrs312262696
geneviewrs312262696
scholarrs312262696
googlers312262696
pharmgkbrs312262696
gwascentralrs312262696
openSNPrs312262696
23andMers312262696
23andMe allrs312262696
SNP Nexus

SNPshotrs312262696
SNPdbers312262696
MSV3drs312262696
GWAS Ctlgrs312262696
Max Magnitude0
ClinVar
Risk rs312262696(A;A)
Alt rs312262696(A;A)
Reference rs312262696(G;G)
Significance Probable-Pathogenic
Disease Atypical hemolytic uremic syndrome
Variation info
Gene DGKE
CLNDBN Atypical hemolytic uremic syndrome
Reversed 0
HGVS NC_000017.10:g.54926056G>A
CLNSRC ClinVar
CLNACC RCV000122616.1,