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: rs56984562
rs56984562
5 0.846 0.179 1 156137666 missense variant C/A,G,T snp 0.810 1.000 7 2004 2016
dbSNP: rs59026483
rs59026483
6 0.821 0.143 1 156134457 missense variant C/T snp 0.810 < 0.001 4 2002 2006
dbSNP: rs28933093
rs28933093
4 0.923 0.071 1 156130741 missense variant G/A snp 0.810 1.000 3 2003 2012
dbSNP: rs28933091
rs28933091
3 0.923 0.143 1 156134474 missense variant C/A,G snp 0.800 5 1993 2013
dbSNP: rs61195471
rs61195471
5 0.846 0.107 1 156134496 missense variant G/A snp 0.800 4 1993 2010
dbSNP: rs28933092
rs28933092
2 1.000 0.036 1 156134497 missense variant A/G,T snp 0.800 3 1999 2008
dbSNP: rs61295588
rs61295588
1 1.000 0.036 1 156134809 missense variant T/C snp 0.800 3 1993 2010
dbSNP: rs267607570
rs267607570
2 0.923 0.107 1 156130757 missense variant G/A,C snp 4.8E-05 0.800 2 2008 2010
dbSNP: rs28928900
rs28928900
2 0.923 0.107 1 156115096 missense variant C/G,T snp 0.800 2 1999 2002
dbSNP: rs28933090
rs28933090
3 0.923 0.143 1 156115172 missense variant T/A,G snp 0.800 2 1999 2002
dbSNP: rs61672878
rs61672878
7 0.801 0.179 1 156136094 missense variant G/A,T snp 0.720 1.000 6 2000 2014
dbSNP: rs60682848
rs60682848
5 0.846 0.143 1 156134838 stop gained C/T snp 0.720 0.500 3 1993 2013
dbSNP: rs267607578
rs267607578
1 1.000 0.036 1 156136952 missense variant G/A snp 0.710 1.000 2 2010 2012
dbSNP: rs57045855
rs57045855
3 1.000 0.036 1 156134464 missense variant A/G,T snp 0.710 1.000 1 2006 2006
dbSNP: rs61661343
rs61661343
4 0.846 0.036 1 156130687 missense variant T/C snp 0.710 1.000 1 2004 2004
dbSNP: rs1057515421
rs1057515421
1 1.000 0.036 1 156136284 stop gained C/T snp 0.700 2 1999 2017
dbSNP: rs56771886
rs56771886
2 0.923 0.143 1 156135923 frameshift variant CT/C in-del 0.700 2 1993 2000
dbSNP: rs56816490
rs56816490
3 0.923 0.107 1 156135913 stop gained G/A,T snp 3.2E-05 0.700 2 2002 2012
dbSNP: rs59040894
rs59040894
2 0.923 0.107 1 156115184 missense variant G/A,T snp 0.700 2 2003 2010
dbSNP: rs80338938
rs80338938
1 1.000 0.036 1 156137756 missense variant C/A,T snp 3.3E-05; 4.7E-05 0.700 2 1993 1999
dbSNP: rs150840924
rs150840924
2 1.000 0.036 1 156136359 missense variant C/T snp 8.0E-06 0.700 1 2004 2004
dbSNP: rs201583907
rs201583907
1 1.000 0.036 1 156137191 missense variant G/A,C snp 8.6E-05 6.4E-05 0.700 1 2012 2012
dbSNP: rs267607560
rs267607560
2 0.923 0.036 1 156115192 missense variant C/T snp 0.700 1 2012 2012
dbSNP: rs267607568
rs267607568
1 1.000 0.036 1 156115220 missense variant G/A,C,T snp 4.1E-06 0.700 1 2010 2010
dbSNP: rs267607572
rs267607572
1 1.000 0.036 1 156134518 missense variant T/G snp 0.700 1 2010 2010