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: rs2039424
rs2039424
2 1.000 0.080 9 68817258 intron variant G/A snv 0.63 0.700 1.000 4 2019 2019
dbSNP: rs4744712
rs4744712
4 1.000 0.080 9 68819791 intron variant A/C;T snv 0.700 1.000 3 2016 2019
dbSNP: rs10746942
rs10746942
2 9 68819549 intron variant G/A snv 0.63 0.700 1.000 2 2017 2019
dbSNP: rs1556751
rs1556751
3 1.000 0.040 9 68818296 intron variant G/A snv 0.63 0.700 1.000 1 2019 2019