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: rs6908042
rs6908042
1 6 20589496 intron variant A/G snv 0.27 0.700 1.000 2 2018 2019
dbSNP: rs17584626
rs17584626
1 6 20560204 intron variant A/T snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs7744833
rs7744833
1 6 20581597 intron variant A/G;T snv 0.700 1.000 1 2019 2019