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: rs111033270
rs111033270
3 0.851 0.200 10 71779316 missense variant G/A snv 6.8E-05 1.6E-04 0.700 0
dbSNP: rs183431253
rs183431253
3 0.882 0.200 10 71790413 missense variant G/A snv 2.9E-05 1.4E-05 0.700 0
dbSNP: rs367928692
rs367928692
3 0.882 0.200 10 71791123 intron variant G/A;T snv 4.9E-05; 4.4E-06 0.700 0
dbSNP: rs397517329
rs397517329
3 0.882 0.200 10 71738597 stop gained C/A;T snv 4.0E-06 0.700 0
dbSNP: rs767004225
rs767004225
1 1.000 10 71734271 missense variant G/A;T snv 6.9E-05 6.3E-05 0.700 0