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: rs763364977
rs763364977
NEB ; RIF1
2 0.925 0.080 2 151496308 stop gained G/A;T snv 8.1E-06 2.1E-05 0.700 0
dbSNP: rs781667543
rs781667543
NEB ; RIF1
2 0.925 0.080 2 151497713 splice acceptor variant -/AACA;ACA delins 8.8E-05; 1.0E-05 2.1E-05 0.700 0
dbSNP: rs80358249
rs80358249
2 0.925 0.080 19 55137176 stop gained C/A snv 4.0E-06 1.6E-04 0.700 0
dbSNP: rs80358250
rs80358250
2 0.925 0.080 14 34713462 missense variant C/T snv 0.700 0
dbSNP: rs928945364
rs928945364
NEB
2 0.925 0.080 2 151617381 stop gained G/A snv 7.0E-06 0.700 0
dbSNP: rs934111355
rs934111355
NEB ; RIF1
2 0.925 0.080 2 151496992 frameshift variant GTAG/- delins 5.0E-06 1.4E-05 0.700 0
dbSNP: rs750900690
rs750900690
NEB ; RIF1
1 1.000 0.080 2 151527528 stop gained G/A snv 8.1E-06 0.700 1.000 4 2002 2015
dbSNP: rs760200697
rs760200697
NEB ; RIF1
1 1.000 0.080 2 151491697 stop gained A/C snv 4.5E-06 0.700 1.000 4 2002 2015
dbSNP: rs1273559032
rs1273559032
1 1.000 0.080 1 229432619 missense variant C/T snv 0.010 1.000 1 2004 2004
dbSNP: rs1373863123
rs1373863123
4 1.000 0.080 7 5529540 missense variant G/A snv 0.010 1.000 1 2013 2013
dbSNP: rs1559168230
rs1559168230
NEB
1 1.000 0.080 2 151679718 splice donor variant TACGTCA/- del 0.700 1.000 1 2014 2014
dbSNP: rs267606626
rs267606626
1 1.000 0.080 1 229432788 missense variant C/A snv 0.010 1.000 1 2009 2009
dbSNP: rs267606627
rs267606627
1 1.000 0.080 1 229432787 missense variant G/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs730881159
rs730881159
1 1.000 0.080 15 63061774 missense variant G/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs886044062
rs886044062
1 1.000 0.080 1 229432087 missense variant C/T snv 0.010 1.000 1 2011 2011
dbSNP: rs1559573882
rs1559573882
NEB
1 1.000 0.080 2 151717504 frameshift variant C/- delins 0.700 0
dbSNP: rs777819332
rs777819332
NEB
1 1.000 0.080 2 151545911 stop gained C/A snv 4.1E-06 0.700 0