Source: BEFREE ×
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: rs2853578
rs2853578
1 1.000 0.120 9 104831027 missense variant T/A;C snv 4.0E-06 7.0E-06 0.810 1.000 1 2008 2008
dbSNP: rs137854496
rs137854496
1 1.000 0.120 9 104831048 missense variant C/A;G snv 5.6E-05; 4.0E-05 0.720 1.000 2 1999 2013
dbSNP: rs137854498
rs137854498
2 1.000 0.120 9 104798504 missense variant G/A;T snv 8.0E-06; 8.0E-06 0.710 1.000 1 1999 2013
dbSNP: rs141021096
rs141021096
1 1.000 0.120 9 104819690 missense variant G/T snv 8.0E-06 0.710 1.000 1 2004 2004
dbSNP: rs374404992
rs374404992
1 1.000 0.120 9 104840489 stop gained G/A snv 8.0E-06 7.0E-06 0.020 1.000 2 2003 2010
dbSNP: rs778885878
rs778885878
1 1.000 0.120 9 104819624 missense variant C/T snv 4.0E-06 0.020 1.000 2 2006 2011
dbSNP: rs1225973801
rs1225973801
1 1.000 0.120 9 104802157 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs575627531
rs575627531
2 1.000 0.120 9 104814211 stop gained G/A snv 0.010 1.000 1 2009 2009