rs1122608, SMARCA4

N. diseases: 8
Source: CURATED ×
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
469 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.820 1.000 3 2011 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
162 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.810 0.500 1 2009 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
627 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.720 1.000 1 2014 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
198 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.710 1.000 1 2014 2014
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
34 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013