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: rs1997995
rs1997995
1 1.000 0.040 6 45406446 intron variant A/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs2396502
rs2396502
1 1.000 0.040 6 45389962 intron variant A/C snv 0.63 0.700 1.000 1 2019 2019