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: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1
0.710 1.000 1 2018 2018
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease
0.710 1.000 1 2018 2018
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2016 2016
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2013 2013
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
Squamous cell carcinoma of esophagus
0.010 < 0.001 1 2014 2014
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2019 2019
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2015 2015
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2014 2014
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2017 2017
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2016 2016
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 < 0.001 1 2010 2010
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0001857
Disease: AIDS related complex
AIDS related complex
0.010 1.000 1 2015 2015
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2013 2013
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2013 2013