rs2070699, EDN1

N. diseases: 14
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.
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
Malignant neoplasm of large intestine
375 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.700 1.000 1 2019 2019
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.020 0.500 2 2013 2014
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.020 0.500 2 2013 2014
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.020 0.500 2 2013 2014
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.010 1.000 1 2013 2013
Respiratory distress
CUI: C0476273
Disease: Respiratory distress
16 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 0.010 1.000 1 2016 2016