Source: CURATED

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: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2013 2013
dbSNP: rs1665650
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2013 2013