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: rs182798226
rs182798226
2 0.925 0.080 6 31271285 missense variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs281860503
rs281860503
1 1.000 0.040 6 31271187 missense variant G/A;C;T snv 0.010 1.000 1 1997 1997
dbSNP: rs281860563
rs281860563
1 1.000 0.040 6 31270363 stop gained G/A;T snv 0.010 1.000 1 1997 1997
dbSNP: rs45580333
rs45580333
1 1.000 0.040 6 31271262 missense variant C/A;G;T snv 4.0E-06 1.5E-05 0.010 1.000 1 1997 1997