CDK14, cyclin dependent kinase 14, 5218

N. diseases: 40; N. variants: 21
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: rs10272859
rs10272859 		0.925 0.120 7 90689160 intron variant G/C snv 0.39
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.710 1.000 1 2018 2018
dbSNP: rs10253488
rs10253488 		1.000 0.040 7 90774401 intron variant G/A snv 0.65
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10272859
rs10272859 		0.925 0.120 7 90689160 intron variant G/C snv 0.39
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2018 2018
dbSNP: rs10274344
rs10274344 		1.000 0.040 7 91208791 3 prime UTR variant C/G snv 7.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10487983
rs10487983 		1.000 0.040 7 90765441 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10953023
rs10953023 		1.000 0.040 7 90791804 intron variant G/A snv 0.64
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10953024
rs10953024 		7 90874752 intron variant T/C snv 0.12
CUI: C0236379
Disease: ESTRONE MEASUREMENT
ESTRONE MEASUREMENT 		0.700 1.000 1 2017 2017
dbSNP: rs10953024
rs10953024 		7 90874752 intron variant T/C snv 0.12
CUI: C0337432
Disease: Androstenedione measurement
Androstenedione measurement 		0.700 1.000 1 2017 2017
dbSNP: rs11763939
rs11763939 		1.000 0.040 7 90770738 intron variant C/G snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11971019
rs11971019 		1.000 0.040 7 90791888 intron variant G/T snv 0.16
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12386665
rs12386665 		1.000 0.040 7 90804120 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12704597
rs12704597 		1.000 0.040 7 91203869 intron variant A/G snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17350639
rs17350639 		1.000 0.040 7 91202912 intron variant A/G snv 0.17
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17394921
rs17394921 		1.000 0.040 7 90795902 intron variant G/A snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17472856
rs17472856 		1.000 0.040 7 90782717 intron variant A/T snv 8.2E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2040519
rs2040519 		1.000 0.040 7 90793919 intron variant G/A snv 0.88
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs3808234
rs3808234 		1.000 0.040 7 90821661 intron variant C/A snv 8.3E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs5009746
rs5009746 		1.000 0.040 7 90828728 intron variant A/G snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs67617547
rs67617547 		7 90667863 intron variant C/G snv 0.28
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs6951213
rs6951213 		1.000 0.040 7 90783786 intron variant G/A snv 0.43
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7780768
rs7780768 		1.000 0.040 7 90770577 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: rs975004
rs975004 		1.000 0.040 7 90971314 intron variant A/G snv 6.9E-02
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs773301216
rs773301216 		1.000 0.040 7 91118066 missense variant G/A snv 4.0E-06 1.4E-05
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
Ovarian Mucinous Adenocarcinoma 		Neoplasms 0.700 0
dbSNP: rs10272859
rs10272859 		0.925 0.120 7 90689160 intron variant G/C snv 0.39
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs10272859
rs10272859 		0.925 0.120 7 90689160 intron variant G/C snv 0.39
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2018 2018