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: rs1883025
rs1883025
7 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs2515629
rs2515629
3 1.000 0.040 9 104832083 intron variant A/G snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs3890182
rs3890182
4 0.925 0.120 9 104885374 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs3905000
rs3905000
3 0.925 0.080 9 104894789 intron variant G/A snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs4149268
rs4149268
4 1.000 0.040 9 104884939 intron variant C/T snv 0.46 0.700 1.000 1 2011 2011