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: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
Liver and Intrahepatic Biliary Tract Carcinoma 		0.020 1.000 2 2017 2019
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2016 2018
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver 		0.020 1.000 2 2017 2019
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2016 2018
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma 		0.020 1.000 2 2017 2019
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
Laryngeal Squamous Cell Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		0.010 1.000 1 2019 2019
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		0.010 1.000 1 2019 2019
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2016 2016
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2016 2016
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2016 2016
dbSNP: rs1682111
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019