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: rs16986890
rs16986890
1 20 37698121 intron variant A/G snv 9.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs6020395
rs6020395
1 20 37710922 intron variant G/C snv 0.16 0.700 1.000 1 2013 2013
dbSNP: rs6020712
rs6020712
4 1.000 0.080 20 37758210 intron variant G/A snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs9679781
rs9679781
1 20 37843596 intron variant A/C;G snv 0.700 1.000 1 2013 2013