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: rs13276026
rs13276026
3 8 10752445 intron variant G/A snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs4551304
rs4551304
3 8 10807559 intron variant A/G snv 0.65 0.700 1.000 1 2018 2018
dbSNP: rs7814757
rs7814757
2 8 10817678 intron variant T/C;G snv 0.700 1.000 1 2018 2018