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: rs116385615
rs116385615
2 1.000 0.040 6 31913532 intron variant T/C snv 0.700 1.000 1 2017 2017
dbSNP: rs142520578
rs142520578
2 1.000 0.040 6 31894038 intron variant G/A snv 0.700 1.000 1 2017 2017
dbSNP: rs2293751
rs2293751
2 1.000 0.040 6 31940060 intron variant G/A;C snv 0.700 1.000 1 2017 2017