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rs869312943

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312943(C;T)
Make rs869312943(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position46372813
GeneDGKZ
is asnp
is mentioned by
dbSNPrs869312943
ebirs869312943
HLIrs869312943
Exacrs869312943
Varsomers869312943
Maprs869312943
PheGenIrs869312943
hapmaprs869312943
1000 genomesrs869312943
hgdprs869312943
ensemblrs869312943
gopubmedrs869312943
geneviewrs869312943
scholarrs869312943
googlers869312943
pharmgkbrs869312943
gwascentralrs869312943
openSNPrs869312943
23andMers869312943
23andMe allrs869312943
SNP Nexus

SNPshotrs869312943
SNPdbers869312943
MSV3drs869312943
GWAS Ctlgrs869312943
Max Magnitude0
ClinVar
Risk rs869312943(T;T)
Alt rs869312943(T;T)
Reference rs869312943(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DGKZ
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.46394363C>T
CLNSRC
CLNACC RCV000210658.1,