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: rs9503598
rs9503598
1 6 3446029 intron variant G/A snv 0.38 0.700 1.000 2 2017 2019
dbSNP: rs11759522
rs11759522
1 6 3450580 intron variant C/G snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs9503599
rs9503599
1 6 3450814 intron variant T/A;C snv 0.700 1.000 1 2018 2018