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: rs3128917
rs3128917
2 0.925 0.200 6 33092219 non coding transcript exon variant T/G snv 0.33 0.720 1.000 4 2009 2019
dbSNP: rs2281388
rs2281388
4 0.851 0.400 6 33092341 non coding transcript exon variant G/A snv 2.6E-02 0.700 1.000 2 2009 2011
dbSNP: rs3117222
rs3117222
3 0.882 0.280 6 33093172 intron variant C/T snv 0.33 0.700 1.000 2 2009 2011
dbSNP: rs2295119
rs2295119
2 0.925 0.120 6 33093093 non coding transcript exon variant G/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs3117216
rs3117216
1 1.000 0.080 6 33095626 intron variant A/G snv 0.38 0.700 1.000 1 2013 2013