DCDC1, doublecortin domain containing 1, 341019

N. diseases: 9; N. variants: 11
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: rs16921914
rs16921914 		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 		1.000 0.040 11 30871277 intron variant A/G snv 0.47
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs163879
rs163879 		11 30930127 intron variant C/T snv 0.62
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 1 2012 2012
dbSNP: rs163879
rs163879 		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 		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 		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 		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 		1.000 0.040 11 30830509 3 prime UTR variant C/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs662735
rs662735 		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 		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 		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
dbSNP: rs111299050
rs111299050 		1.000 0.080 11 31370815 missense variant A/G snv 4.3E-04 2.2E-03
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs672931
rs672931 		1.000 0.040 11 30899350 intron variant T/C snv 0.50
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs672931
rs672931 		1.000 0.040 11 30899350 intron variant T/C snv 0.50
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2018 2018