rs11884596, LOC105373831

N. diseases: 10
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.
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
Malignant neoplasm of large intestine
375 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.776 0.080 2 198747683 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019