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: rs706779
rs706779
1 0.827 0.160 10 6056861 intron variant T/C snv 0.48 0.810 1.000 3 2010 2016