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: rs121908838
rs121908838
1 1.000 0.080 3 189864349 missense variant A/G snv 0.800 1.000 2 2000 2001
dbSNP: rs886039442
rs886039442
2 0.925 0.160 3 189867906 missense variant G/A snv 0.700 1.000 2 2000 2001
dbSNP: rs121908839
rs121908839
2 0.925 0.160 3 189867905 missense variant C/T snv 0.700 0
dbSNP: rs121908848
rs121908848
2 0.925 0.080 3 189738739 missense variant C/A;T snv 1.2E-05 0.700 0