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: rs1167204443
rs1167204443
3 0.882 0.160 2 170829475 missense variant G/C snv 4.0E-06 1.4E-05 0.020 0.500 2 1999 2003
dbSNP: rs1190356035
rs1190356035
4 0.882 0.360 2 170853979 missense variant G/A snv 7.0E-06 0.010 1.000 1 2000 2000