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: rs587776829
rs587776829
3 0.878 0.179 20 58909196 frameshift variant TGACT/T in-del 0.700 6 1992 2008
dbSNP: rs797045046
rs797045046
2 0.923 0.107 20 58891760 stop gained C/G,T snp 5.0E-06 0.700 5 2001 2017
dbSNP: rs137854538
rs137854538
2 0.923 0.107 20 58909553 missense variant G/A snp 0.700 3 1996 2001
dbSNP: rs137854532
rs137854532
4 0.846 0.143 20 58905443 missense variant C/T snp 0.700 2 1993 2015
dbSNP: rs1135401777
rs1135401777
2 0.923 0.107 20 58853740 missense variant G/A snp 0.700 1 2015 2015
dbSNP: rs137854530
rs137854530
1 1.000 0.107 20 58891727 start lost A/G,T snp 0.700 1 1990 1990
dbSNP: rs137854534
rs137854534
2 0.923 0.107 20 58909715 missense variant C/G snp 0.700 1 1998 1998
dbSNP: rs137854539
rs137854539
3 0.878 0.107 20 58903703 missense variant C/T snp 0.700 1 2001 2001
dbSNP: rs863224876
rs863224876
2 0.923 0.107 20 58909991 stop gained C/T snp 0.700 1 2014 2014
dbSNP: rs137854531
rs137854531
2 0.923 0.107 20 58903569 missense variant T/C snp 0.700 0
dbSNP: rs397514456
rs397514456
3 0.878 0.107 20 58910818 stop gained G/A,T snp 0.700 0