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: rs141234028
rs141234028
1 2 143570965 intron variant C/T snv 7.7E-03 0.700 1.000 1 2019 2019
dbSNP: rs74847330
rs74847330
4 2 143074030 intergenic variant A/G snv 8.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs79716587
rs79716587
3 2 143129250 intron variant G/A snv 7.9E-02 0.700 1.000 1 2016 2016