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: rs72823641
rs72823641
4 0.882 0.080 2 102319699 intron variant T/A;C snv 0.700 1.000 2 2019 2019
dbSNP: rs10208293
rs10208293
4 0.882 0.160 2 102349850 intron variant G/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs1861245
rs1861245
2 0.925 0.080 2 102350446 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs4988958
rs4988958
2 1.000 0.080 2 102351825 synonymous variant T/C snv 0.34 0.46 0.700 1.000 1 2018 2018