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: rs11112992
rs11112992
1.000 0.040 12 106435501 intron variant T/C snv 0.20
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013