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: rs2227127
rs2227127
2 0.925 0.120 6 32744005 intron variant A/G snv 0.37 0.700 1.000 1 2009 2009
dbSNP: rs2239800
rs2239800
3 0.882 0.280 6 32745490 intron variant A/G snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs9272723
rs9272723
2 0.925 0.200 6 32641650 intron variant T/C snv 0.700 1.000 1 2009 2009
dbSNP: rs9276440
rs9276440
2 0.925 0.120 6 32747006 3 prime UTR variant A/G;T snv 0.700 1.000 1 2009 2009