Source: GWASCAT

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: rs11080107
rs11080107
ANKRD13B
1.000 0.040 17 29611406 intron variant T/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs13723
rs13723
CORO6 ; ANKRD13B
1.000 0.040 17 29614868 3 prime UTR variant A/G snv 0.60
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs7220401
rs7220401
ANKRD13B
1.000 0.040 17 29608670 non coding transcript exon variant T/C snv 0.55
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018