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: rs1466662
rs1466662
1 1.000 0.080 4 154426241 intron variant A/T snv 0.28 0.810 1.000 1 2012 2016
dbSNP: rs12500118
rs12500118
1 1.000 0.080 4 154423482 intron variant C/T snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs4696572
rs4696572
1 1.000 0.080 4 154433764 intron variant T/C;G snv 0.29 0.700 1.000 1 2012 2012