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: rs10489844
rs10489844
1 1 158758599 intron variant C/T snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs1864346
rs1864346
1 1 158766655 missense variant C/T snv 0.31 0.25 0.700 1.000 1 2011 2011
dbSNP: rs1864347
rs1864347
1 1 158766727 intron variant A/G;T snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs454127
rs454127
1 1 158750398 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs857854
rs857854
1 1 158794193 upstream gene variant T/C snv 0.66 0.700 1.000 1 2011 2011
dbSNP: rs857859
rs857859
1 1 158801660 intergenic variant T/A;C snv 0.700 1.000 1 2011 2011