Source: ALL

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: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.720 1.000 3 2014 2018
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2011 2011
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 1.000 2 2014 2018
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2018 2018