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: rs17073759
rs17073759
2 0.925 0.040 3 65777801 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs7633294
rs7633294
2 0.925 0.040 3 65650810 intron variant A/G snv 0.71 0.700 1.000 1 2017 2017