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: rs347685
rs347685
4 1.000 0.080 3 142088295 intron variant C/A snv 0.74 0.700 1.000 2 2010 2016
dbSNP: rs2861422
rs2861422
2 3 142005802 intron variant C/T snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs7640665
rs7640665
2 3 142094330 intron variant G/A;C;T snv 0.700 1.000 1 2017 2017