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: rs17114036
rs17114036
5 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.800 1.000 2 2011 2014
dbSNP: rs17114046
rs17114046
2 0.925 0.040 1 56500678 intron variant A/G snv 0.12 0.800 1.000 2 2011 2011
dbSNP: rs2404715
rs2404715
2 1.000 0.040 1 56543106 intron variant C/T snv 7.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs12566304
rs12566304
1 1.000 0.040 1 56570684 intron variant C/A snv 0.28 0.010 1.000 1 2017 2017
dbSNP: rs1759752
rs1759752
1 1.000 0.040 1 56527743 intron variant G/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs1930760
rs1930760
1 1.000 0.040 1 56541867 intron variant T/C snv 0.42 0.010 1.000 1 2017 2017
dbSNP: rs72664392
rs72664392
1 1.000 0.040 1 56580502 intron variant T/C snv 2.2E-02 0.010 1.000 1 2018 2018