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: rs104894086
rs104894086
2 1.000 0.200 8 38146068 missense variant C/A;T snv 0.010 1.000 1 2001 2001
dbSNP: rs1315425582
rs1315425582
1 8 38150817 start lost A/C snv 7.0E-06 0.010 1.000 1 2001 2001