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: rs11817730
rs11817730
1 10 97598754 intron variant A/G snv 0.18 0.20 0.700 1.000 1 2012 2012
dbSNP: rs2297644
rs2297644
1 10 97599982 non coding transcript exon variant T/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs2861970
rs2861970
1 10 97592327 intron variant A/C;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs61863282
rs61863282
1 10 97591247 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs7068278
rs7068278
1 10 97597385 intron variant G/T snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs7078003
rs7078003
3 10 97599655 non coding transcript exon variant C/T snv 0.14 0.14 0.700 1.000 1 2012 2012
dbSNP: rs7913812
rs7913812
1 10 97597874 intron variant T/C snv 0.20 0.700 1.000 1 2012 2012