DGKD, diacylglycerol kinase delta, 8527

N. diseases: 18; N. variants: 37
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6722763
rs6722763 		2 233373564 intron variant A/C;G snv
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 1 2009 2009
dbSNP: rs6722763
rs6722763 		2 233373564 intron variant A/C;G snv
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2009 2009
dbSNP: rs1441093
rs1441093 		2 233363838 intron variant A/G snv 0.82
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2009 2009
dbSNP: rs1441093
rs1441093 		2 233363838 intron variant A/G snv 0.82
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 1 2009 2009
dbSNP: rs3754595
rs3754595 		2 233461779 intron variant A/G snv 0.17
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 1 2009 2009
dbSNP: rs3754595
rs3754595 		2 233461779 intron variant A/G snv 0.17
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2009 2009
dbSNP: rs6714168
rs6714168 		2 233431353 intron variant A/G snv 0.31
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2009 2009
dbSNP: rs6714168
rs6714168 		2 233431353 intron variant A/G snv 0.31
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 1 2009 2009
dbSNP: rs7587876
rs7587876 		2 233407386 intron variant A/G snv 0.12
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 1 2009 2009
dbSNP: rs7587876
rs7587876 		2 233407386 intron variant A/G snv 0.12
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2009 2009
dbSNP: rs838721
rs838721 		2 233394759 intron variant A/G snv 0.64
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs838720
rs838720 		1.000 0.080 2 233394635 intron variant C/A;G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs838709
rs838709 		2 233376098 intron variant C/A;T snv
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2009 2009
dbSNP: rs838709
rs838709 		2 233376098 intron variant C/A;T snv
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 1 2009 2009
dbSNP: rs1550532
rs1550532 		2 233356202 intron variant C/G snv 0.75
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.800 1.000 3 2009 2010
dbSNP: rs1550532
rs1550532 		2 233356202 intron variant C/G snv 0.75
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 2 2009 2009
dbSNP: rs1550532
rs1550532 		2 233356202 intron variant C/G snv 0.75
CUI: C0201925
Disease: Calcium measurement
Calcium measurement 		0.800 1.000 1 2013 2013
dbSNP: rs1550532
rs1550532 		2 233356202 intron variant C/G snv 0.75
CUI: C0428302
Disease: Calcium level result
Calcium level result 		0.700 1.000 1 2013 2013
dbSNP: rs7576633
rs7576633 		2 233370606 intron variant C/G snv 0.23
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2009 2009
dbSNP: rs7576633
rs7576633 		2 233370606 intron variant C/G snv 0.23
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 1 2009 2009
dbSNP: rs2242100
rs2242100 		2 233449640 intron variant C/T snv 0.72
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 1 2009 2009
dbSNP: rs2242100
rs2242100 		2 233449640 intron variant C/T snv 0.72
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2009 2009
dbSNP: rs34339006
rs34339006 		1.000 0.040 2 233362876 intron variant C/T snv 0.32
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs34339006
rs34339006 		1.000 0.040 2 233362876 intron variant C/T snv 0.32
CUI: C0201925
Disease: Calcium measurement
Calcium measurement 		0.700 1.000 1 2018 2018
dbSNP: rs838708
rs838708 		2 233375753 intron variant G/A snv 0.74
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 2 2009 2009