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: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C1261473
Disease: Sarcoma
Sarcoma 		0.010 1.000 1 2018 2018
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
Malignant neoplasm of soft tissue 		0.010 1.000 1 2018 2018
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0278607
Disease: Adult Leiomyosarcoma
Adult Leiomyosarcoma 		0.010 1.000 1 2018 2018
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0279986
Disease: Childhood Leiomyosarcoma
Childhood Leiomyosarcoma 		0.010 1.000 1 2018 2018
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0023269
Disease: leiomyosarcoma
leiomyosarcoma 		0.010 1.000 1 2018 2018
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma 		0.010 1.000 1 2017 2017