rs10411210, RHPN2

N. diseases: 13
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.840 1.000 7 2008 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.710 1.000 4 2008 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
Malignant neoplasm of large intestine
375 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
Malignant neoplasm of colon and/or rectum
502 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.020 1.000 2 2015 2015
Alcohol or Other Drugs use
CUI: C0237123
Disease: Alcohol or Other Drugs use
21 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.010 1.000 1 2012 2012
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.010 1.000 1 2013 2013
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 1 2010 2010