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: rs121908450
rs121908450
4 0.851 0.160 2 108929288 missense variant C/T snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs780424781
rs780424781
2 0.925 0.080 2 108929289 missense variant G/A;T snv 8.0E-06 7.0E-06 0.700 0