Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16921914
rs16921914
DCDC1
11 31189224 intron variant G/A snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs1448938
rs1448938
DCDC1 ; LOC105376611
1.000 0.040 11 30871277 intron variant A/G snv 0.47
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2019 2019
dbSNP: rs163879
rs163879
DCDC1
11 30930127 intron variant C/T snv 0.62
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2012 2012
dbSNP: rs208079
rs208079
DCDC1
11 31106605 intron variant C/G snv 0.52
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs273573
rs273573
DCDC1 ; LOC105376611
11 30889444 intron variant A/C snv 0.69
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs2761589
rs2761589
DCDC1
11 31289882 intron variant C/A;G;T snv
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		0.700 1.000 1 2019 2019
dbSNP: rs620339
rs620339
DCDC1 ; LOC107984419
1.000 0.040 11 30830509 3 prime UTR variant C/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2016 2016
dbSNP: rs662735
rs662735
DCDC1 ; LOC105376611
11 30881895 intron variant T/A;G snv
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs662735
rs662735
DCDC1 ; LOC105376611
11 30881895 intron variant T/A;G snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs919045
rs919045
DCDC1
11 31090263 intron variant T/C snv 0.30
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018