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: rs28840750
rs28840750
RHPN2
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs28840750
rs28840750
RHPN2
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs28840750
rs28840750
RHPN2
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs28840750
rs28840750
RHPN2
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
RHPN2
0.790 0.080 19 33034013 intron variant T/G snv 0.13
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs10411210
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.020 1.000 2 2015 2015
dbSNP: rs10411210
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C0237123
Disease: Alcohol or Other Drugs use
Alcohol or Other Drugs use 		0.010 1.000 1 2012 2012
dbSNP: rs10411210
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2013 2013