AKT2, AKT serine/threonine kinase 2, 208

N. diseases: 264; N. variants: 18
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: rs16974157
rs16974157
1.000 0.040 19 40267017 intron variant C/A snv 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs3730050
rs3730050
19 40265075 intron variant T/C snv 0.73
CUI: C0686377
Disease: CNS metastases
CNS metastases
Neoplasms; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3730051
rs3730051
1.000 0.120 19 40238790 intron variant T/C snv 0.24
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs7247515
rs7247515
0.925 0.080 19 40250008 intron variant C/T snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs7247515
rs7247515
0.925 0.080 19 40250008 intron variant C/T snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7250897
rs7250897
0.882 0.080 19 40277326 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7250897
rs7250897
0.882 0.080 19 40277326 intron variant T/A;C snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7250897
rs7250897
0.882 0.080 19 40277326 intron variant T/A;C snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs8100018
rs8100018
1.000 0.120 19 40246116 intron variant C/A;G snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs892119
rs892119
0.925 0.080 19 40254165 intron variant C/T snv 0.19
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012
dbSNP: rs892119
rs892119
0.925 0.080 19 40254165 intron variant C/T snv 0.19
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012
dbSNP: rs969531
rs969531
1.000 0.040 19 40272959 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9710247
rs9710247
19 40254542 intron variant A/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C0023418
Disease: leukemia
leukemia
Neoplasms 0.020 1.000 2 2007 2008
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 1.000 2 2007 2008
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.020 1.000 2 2008 2008
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY
0.800 1.000 1 2011 2011
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs387906659
rs387906659
0.742 0.280 19 40257052 stop gained C/A;T snv
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
Neoplasms 0.010 1.000 1 2007 2007