Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13361707
rs13361707
PRKAA1
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.780 1.000 8 2011 2018
dbSNP: rs13361707
rs13361707
PRKAA1
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.780 1.000 8 2011 2018
dbSNP: rs13361707
rs13361707
PRKAA1
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2016 2018
dbSNP: rs13361707
rs13361707
PRKAA1
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2016 2018
dbSNP: rs13361707
rs13361707
PRKAA1
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia 		0.010 1.000 1 2017 2017
dbSNP: rs13361707
rs13361707
PRKAA1
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2019 2019