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: rs11019128
rs11019128
1 11 90660419 intron variant C/T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs34226552
rs34226552
1 11 90676187 intron variant G/A snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs7127743
rs7127743
1 11 90661372 intron variant T/C snv 0.45 0.700 1.000 1 2018 2018