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: rs5742626
rs5742626
3 12 102464131 intron variant T/C snv 2.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs5742663
rs5742663
1 12 102430212 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs5742683
rs5742683
1 12 102419939 intron variant A/G snv 3.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs7300373
rs7300373
1 12 102438008 intron variant T/G snv 1.4E-02 0.700 1.000 1 2012 2012