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: rs3131294
rs3131294
1 1.000 0.080 6 32212369 intron variant A/G snv 0.91 0.700 1.000 1 2007 2007
dbSNP: rs3132946
rs3132946
3 0.882 0.240 6 32222251 intron variant A/G snv 0.91 0.700 1.000 1 2010 2010
dbSNP: rs438475
rs438475
1 1.000 0.080 6 32218468 intron variant G/A;C snv 0.700 1.000 1 2007 2007