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: rs121908845
rs121908845
2 0.925 0.200 3 189889478 missense variant T/C snv 0.810 1.000 4 2003 2010
dbSNP: rs121908840
rs121908840
2 0.925 0.160 3 189867903 missense variant G/A snv 0.800 1.000 3 2003 2004
dbSNP: rs121908846
rs121908846
1 1.000 0.160 3 189890874 missense variant T/C;G snv 4.0E-06 0.800 1.000 3 2003 2004