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: rs3769528
rs3769528
2 2 33246125 intron variant A/G snv 1.1E-02 0.700 1.000 3 2010 2019
dbSNP: rs1545552
rs1545552
2 2 33135271 intron variant A/G;T snv 0.700 1.000 2 2013 2017
dbSNP: rs6714546
rs6714546
2 2 33136358 intron variant A/G snv 0.78 0.700 1.000 2 2010 2014
dbSNP: rs17567417
rs17567417
2 1.000 0.040 2 33205536 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs4670256
rs4670256
1 2 33135489 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs4670893
rs4670893
1 2 33135781 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs6739725
rs6739725
1 2 33281290 intron variant G/A snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs6743685
rs6743685
1 2 33164528 intron variant A/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs72793778
rs72793778
1 2 33133616 intron variant C/G snv 0.17 0.700 1.000 1 2017 2017