DCLK1, doublecortin like kinase 1, 9201

N. diseases: 123; N. variants: 17
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: rs1171052
rs1171052 		1.000 0.040 13 35924961 intron variant T/C snv 0.78
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1171072
rs1171072 		1.000 0.040 13 35927894 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1171091
rs1171091 		1.000 0.040 13 35935910 intron variant G/A snv 9.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1171092
rs1171092 		1.000 0.040 13 35935591 intron variant T/C snv 0.75
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs138712069
rs138712069 		1.000 0.080 13 35897512 intron variant G/A;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6563164
rs6563164 		13 35796291 intron variant G/A snv 0.15
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs6563210
rs6563210 		13 35902310 intron variant A/G snv 0.31
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2011 2011
dbSNP: rs6563210
rs6563210 		13 35902310 intron variant A/G snv 0.31
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs73176188
rs73176188 		13 35826161 intron variant A/G snv 0.13
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7319248
rs7319248 		1.000 0.040 13 35923951 intron variant T/C snv 5.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7358881
rs7358881 		1.000 0.040 13 35933515 intron variant T/C snv 0.53
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs8000101
rs8000101 		13 35826605 intron variant A/G snv 0.12
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs9565689
rs9565689 		1.000 0.040 13 35935497 intron variant A/G snv 2.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9574926
rs9574926 		1.000 0.040 13 35924219 intron variant A/G snv 0.65
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9593571
rs9593571 		1.000 0.040 13 35927838 intron variant C/T snv 0.62
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1366698690
rs1366698690 		1.000 0.080 13 36125860 missense variant C/T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1926320
rs1926320 		0.925 0.040 13 36078480 intron variant T/C snv 0.27
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma 		Eye Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs1926320
rs1926320 		0.925 0.040 13 36078480 intron variant T/C snv 0.27
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		Eye Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs7989807
rs7989807 		0.925 0.040 13 36050952 intron variant C/T snv 0.20
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs7989807
rs7989807 		0.925 0.040 13 36050952 intron variant C/T snv 0.20
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2012 2012