Source: GWASDB

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: rs1122608
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.820 1.000 2 2011 2016
dbSNP: rs11669133
rs11669133
SMARCA4
1.000 0.040 19 10981463 intron variant G/A snv 4.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs73013202
rs73013202
SMARCA4
1.000 0.040 19 11069033 intron variant C/G snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012