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: rs2245368
rs2245368
3 7 76978826 non coding transcript exon variant C/T snv 0.80 0.700 1.000 5 2015 2018
dbSNP: rs17149254
rs17149254
1 7 77005146 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs2430307
rs2430307
2 7 76980627 non coding transcript exon variant T/C snv 0.79 0.700 1.000 1 2017 2017
dbSNP: rs6951489
rs6951489
1 7 77010522 intron variant A/G snv 0.78 0.700 1.000 1 2019 2019
dbSNP: rs6954694
rs6954694
1 7 77002781 intron variant G/A;C snv 0.700 1.000 1 2019 2019