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: rs9841616
rs9841616
1 1.000 0.040 3 181449797 intron variant T/A snv 0.26 0.700 1.000 4 2014 2019
dbSNP: rs9859557
rs9859557
1 1.000 0.040 3 181113122 intron variant A/T snv 0.22 0.700 1.000 2 2017 2019
dbSNP: rs1878874
rs1878874
1 1.000 0.040 3 181317582 intron variant A/C;T snv 0.700 1.000 1 2015 2015