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: rs2048161
rs2048161
ZNF827
4 145932013 intron variant A/C;G snv
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		0.800 1.000 1 2012 2012
dbSNP: rs4547811
rs4547811
ZNF827
4 145873469 intron variant T/C snv 0.20
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs4835265
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.700 1.000 2 2011 2018
dbSNP: rs11930385
rs11930385
ZNF827
4 145924600 intron variant C/T snv 0.51
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12331851
rs12331851
ZNF827
1.000 0.040 4 145928143 intron variant G/A snv 7.1E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.700 1.000 1 2012 2012
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C0037274
Disease: Dermatologic disorders
Dermatologic disorders 		0.700 1.000 1 2018 2018
dbSNP: rs12646351
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 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 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 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 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18
CUI: C0037274
Disease: Dermatologic disorders
Dermatologic disorders 		0.700 1.000 1 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 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 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 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 2018 2018
dbSNP: rs17806780
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2018 2018