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: rs17810546
rs17810546
7 0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 0.820 1.000 4 2008 2020
dbSNP: rs1353248
rs1353248
2 0.925 0.120 3 159905770 intron variant C/T snv 0.32 0.800 1.000 1 2011 2011
dbSNP: rs2561288
rs2561288
1 1.000 0.080 3 159957140 intron variant T/C snv 0.54 0.800 1.000 1 2011 2011
dbSNP: rs76830965
rs76830965
3 0.925 0.120 3 159919889 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9873580
rs9873580
1 1.000 0.080 3 159911578 non coding transcript exon variant C/T snv 9.6E-02 0.700 1.000 1 2016 2016