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: rs1794280
rs1794280
2 1.000 0.080 6 32699394 intergenic variant A/T snv 9.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs2395185
rs2395185
17 0.724 0.360 6 32465390 intron variant G/T snv 0.29 0.700 1.000 1 2014 2014
dbSNP: rs492899
rs492899
4 0.882 0.240 6 31965741 intron variant T/C snv 0.12 0.15 0.700 1.000 1 2019 2019