Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10806425
rs10806425
5 0.851 0.280 6 90216893 intron variant C/A snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs1847472
rs1847472
3 0.807 0.200 6 90263440 intron variant C/A snv 0.25 0.700 1.000 1 2011 2011