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: rs6026584
rs6026584
3 0.925 0.040 20 58894018 intron variant T/C snv 0.70 0.800 1.000 1 2012 2012
dbSNP: rs6026578
rs6026578
4 20 58888417 5 prime UTR variant C/G snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs6026580
rs6026580
1 20 58893095 intron variant C/T snv 0.68 0.700 1.000 1 2019 2019