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: rs104893685
rs104893685
3 0.882 0.040 3 133450432 missense variant C/A;T snv 4.0E-06; 2.0E-05 0.010 1.000 1 2000 2000
dbSNP: rs377423839
rs377423839
2 0.925 0.080 3 133400418 missense variant G/A snv 5.2E-05 1.4E-05 0.010 1.000 1 2014 2014
dbSNP: rs930526408
rs930526408
2 0.925 0.040 3 133472412 missense variant G/A;T snv 0.010 1.000 1 2008 2008