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: rs9282541
rs9282541
2 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 0.800 1.000 2 2008 2019
dbSNP: rs2515629
rs2515629
3 1.000 0.040 9 104832083 intron variant A/G snv 0.16 0.800 1.000 1 2011 2019
dbSNP: rs2575876
rs2575876
4 9 104903458 intron variant G/A snv 0.24 0.800 1.000 1 2012 2019
dbSNP: rs3905000
rs3905000
3 0.925 0.080 9 104894789 intron variant G/A snv 0.14 0.800 1.000 1 2009 2019