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: rs1292048
rs1292048
2 17 59877710 intron variant A/G snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs201184664
rs201184664
2 17 59873258 intron variant -/GT delins 0.700 1.000 1 2017 2017
dbSNP: rs2526358
rs2526358
3 17 59865224 intron variant A/G snv 0.16 0.700 1.000 1 2019 2019