rs13361707, PRKAA1

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.882 0.120 5 40791782 intron variant C/T snv 0.31 0.780 1.000 11 2011 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.882 0.120 5 40791782 intron variant C/T snv 0.31 0.780 1.000 9 2011 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.882 0.120 5 40791782 intron variant C/T snv 0.31 0.700 1.000 1 2011 2011
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.882 0.120 5 40791782 intron variant C/T snv 0.31 0.020 1.000 2 2016 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.882 0.120 5 40791782 intron variant C/T snv 0.31 0.020 1.000 2 2016 2018
Intestinal metaplasia
CUI: C0334037
Disease: Intestinal metaplasia
24 0.882 0.120 5 40791782 intron variant C/T snv 0.31 0.010 1.000 1 2017 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.882 0.120 5 40791782 intron variant C/T snv 0.31 0.010 1.000 1 2019 2019