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: rs12565727
rs12565727
7 0.807 0.080 1 10973025 intron variant A/G snv 0.31 0.800 1.000 1 2012 2012
dbSNP: rs11121667
rs11121667
1 1.000 0.080 1 10978419 intron variant C/T snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs11576658
rs11576658
2 0.925 0.120 1 10977679 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs2003046
rs2003046
2 0.925 0.120 1 10972770 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2095921
rs2095921
7 0.807 0.080 1 10973265 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7542158
rs7542158
1 1.000 0.080 1 10980136 intron variant G/A snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs7542354
rs7542354
7 0.807 0.080 1 10980328 intron variant G/A snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs9430158
rs9430158
1 1.000 0.080 1 10983804 upstream gene variant G/C snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs9659356
rs9659356
1 1.000 0.080 1 10974760 intron variant A/G snv 0.34 0.700 1.000 1 2012 2012