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: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
Malignant neoplasm of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs35446936
rs35446936
0.776 0.080 3 169768720 intron variant G/A snv 0.21
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
0.700 1.000 1 2019 2019