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: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.710 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
Malignant neoplasm of large intestine
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2017 2017
dbSNP: rs56848936
rs56848936
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2017 2017