rs1665650, HSPA12A

N. diseases: 12
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.800 1.000 1 2013 2013
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.700 1.000 1 2013 2013
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.700 1.000 1 2013 2013
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.700 1.000 1 2013 2013
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.700 1.000 1 2013 2013
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.700 1.000 1 2013 2013
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.700 1.000 1 2013 2013
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
375 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.700 1.000 1 2013 2013
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.700 1.000 1 2013 2013
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.010 1.000 1 2017 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.010 1.000 1 2015 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.752 0.160 10 116727589 intron variant T/C snv 0.69 0.010 1.000 1 2015 2015