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: rs2244012
rs2244012
1 1.000 0.080 5 132565533 intron variant A/G snv 0.33 0.820 1.000 3 2010 2016
dbSNP: rs6871536
rs6871536
5 0.827 0.160 5 132634182 intron variant T/C snv 0.24 0.710 1.000 4 2010 2016
dbSNP: rs2040704
rs2040704
1 1.000 0.080 5 132637485 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2240032
rs2240032
1 1.000 0.080 5 132641435 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2299012
rs2299012
2 0.925 0.080 5 132581248 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2706362
rs2706362
1 1.000 0.080 5 132589495 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs17772583
rs17772583
2 0.925 0.120 5 132617818 intron variant A/G snv 0.18 0.010 < 0.001 1 2016 2016
dbSNP: rs2706347
rs2706347
1 1.000 0.080 5 132569425 intron variant G/T snv 0.32 0.010 1.000 1 2011 2011
dbSNP: rs3798134
rs3798134
1 1.000 0.080 5 132629487 intron variant G/A snv 0.26 0.010 < 0.001 1 2016 2016