Source: BEFREE

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: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 1.000 3 2014 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.030 1.000 3 2014 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 1.000 3 2012 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.030 1.000 3 2012 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2019 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 < 0.001 1 2019 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C0023418
Disease: leukemia
leukemia
0.010 1.000 1 2019 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.010 1.000 1 2019 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs3116496
rs3116496
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2018 2018