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: rs11786677
rs11786677
2 8 10406750 intron variant A/G snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs11993089
rs11993089
1 8 10152442 intron variant G/T snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs2062331
rs2062331
2 8 10122482 intron variant A/G snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs34919878
rs34919878
2 8 10241994 intron variant G/A snv 0.29 0.700 1.000 1 2018 2018