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: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.040 0.500 4 2010 2019
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.020 1.000 2 2012 2015
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.020 1.000 2 2014 2015
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.010 1.000 1 2018 2018
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
Secondary malignant neoplasm of colon and/or rectum
0.010 1.000 1 2015 2015
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2013 2013
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0023530
Disease: Leukopenia
Leukopenia
0.010 < 0.001 1 2013 2013
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0009782
Disease: Connective Tissue Diseases
Connective Tissue Diseases
0.010 1.000 1 2014 2014
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0027947
Disease: Neutropenia
Neutropenia
0.010 < 0.001 1 2013 2013
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 < 0.001 1 2013 2013
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2014 2014
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2015 2015
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 < 0.001 1 2013 2013
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2018 2018
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension
0.010 < 0.001 1 2010 2010
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0565599
Disease: Maternal hypertension
Maternal hypertension
0.010 < 0.001 1 2010 2010
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.010 1.000 1 2015 2015
dbSNP: rs776746
rs776746
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013