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: rs3118905
rs3118905
2 13 50531198 intron variant G/A snv 0.21 0.700 1.000 3 2010 2019
dbSNP: rs3118906
rs3118906
2 13 50532652 intron variant G/A snv 0.21 0.700 1.000 3 2013 2019
dbSNP: rs3116602
rs3116602
2 13 50537219 intron variant T/G snv 0.15 0.700 1.000 2 2008 2019
dbSNP: rs1239704
rs1239704
1 13 50578475 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1239948
rs1239948
3 13 50532386 intron variant A/T snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs3116614
rs3116614
1 13 50576594 intron variant A/C snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs3118077
rs3118077
1 13 50728174 intron variant G/A snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs3118914
rs3118914
2 13 50542765 intron variant G/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs3118917
rs3118917
1 13 50571933 intron variant C/A;T snv 3.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs386363597
rs386363597
1 13 50657252 intron variant -/C delins 1.4E-05 0.700 1.000 1 2017 2017
dbSNP: rs475883
rs475883
1 13 50599596 intron variant G/C snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs978332
rs978332
1 13 50562603 intron variant C/T snv 0.69 0.700 1.000 1 2017 2017