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: C1302401
Disease: Adenoma of large intestine
Adenoma 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: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		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: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma 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: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		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: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		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: 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: rs13343954
rs13343954
RHPN2
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
RHPN2
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
RHPN2
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
RHPN2
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
RHPN2
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
RHPN2
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2014 2014