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: rs2030323
rs2030323
3 0.925 0.080 11 27706992 intron variant A/C snv 0.83 0.800 1.000 1 2013 2013
dbSNP: rs10835211
rs10835211
1 1.000 0.080 11 27679818 intron variant G/A snv 0.19 0.700 1.000 1 2013 2013