Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
Malignant neoplasm of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
CUI: C0014170
Disease: Endometrial Neoplasms
Endometrial Neoplasms
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2015 2015
dbSNP: rs10457678
rs10457678
0.790 0.080 6 138801103 intron variant A/G snv 0.19
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs2698744
rs2698744
0.925 0.040 6 138864560 intron variant T/C snv 0.70
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs2698744
rs2698744
0.925 0.040 6 138864560 intron variant T/C snv 0.70
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018