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: 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: rs3730256
rs3730256
1.000 0.080 19 40255305 splice region variant G/A snv 8.4E-02 9.7E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs7254617
rs7254617
0.882 0.120 19 40285605 upstream gene variant G/A;C;T snv
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs7254617
rs7254617
0.882 0.120 19 40285605 upstream gene variant G/A;C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs7254617
rs7254617
0.882 0.120 19 40285605 upstream gene variant G/A;C;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2012 2012
dbSNP: rs7254617
rs7254617
0.882 0.120 19 40285605 upstream gene variant G/A;C;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs7254617
rs7254617
0.882 0.120 19 40285605 upstream gene variant G/A;C;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2304186
rs2304186
0.925 0.160 19 40233814 3 prime UTR variant G/T snv 0.39
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs2304186
rs2304186
0.925 0.160 19 40233814 3 prime UTR variant G/T snv 0.39
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
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: 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: rs1057519754
rs1057519754
19 40236313 missense variant T/C snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 2 2005 2014
dbSNP: rs11880261
rs11880261
1.000 0.040 19 40282734 5 prime UTR variant T/C snv 0.76
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