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: rs6918631
rs6918631
ZSCAN31
1.000 0.040 6 28344679 intron variant C/T snv 5.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012
dbSNP: rs9295769
rs9295769
ZSCAN31
1.000 0.040 6 28336792 splice region variant A/G snv 5.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012