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: rs57045855
rs57045855
6 0.882 0.040 1 156134464 missense variant A/G;T snv 0.720 1.000 18 1999 2012
dbSNP: rs61661343
rs61661343
4 0.851 0.040 1 156130687 missense variant T/C snv 0.720 1.000 18 1999 2019
dbSNP: rs201583907
rs201583907
2 0.925 0.040 1 156137191 missense variant G/A;C snv 8.6E-05 0.700 1.000 17 1999 2012
dbSNP: rs267607560
rs267607560
2 0.925 0.040 1 156115192 missense variant C/T snv 7.0E-06 0.700 1.000 17 1999 2012
dbSNP: rs267607568
rs267607568
1 1.000 0.040 1 156115220 missense variant G/A;C;T snv 4.1E-06 0.700 1.000 17 1999 2012
dbSNP: rs267607572
rs267607572
1 1.000 0.040 1 156134518 missense variant T/G snv 0.700 1.000 17 1999 2012
dbSNP: rs267607574
rs267607574
1 1.000 0.040 1 156135916 missense variant G/A snv 1.6E-05 1.4E-05 0.700 1.000 17 1999 2012
dbSNP: rs28933092
rs28933092
2 1.000 0.040 1 156134497 missense variant A/G;T snv 0.800 1.000 17 1999 2012
dbSNP: rs58789393
rs58789393
1 1.000 0.040 1 156136010 missense variant G/A;T snv 4.0E-06 0.700 1.000 17 1999 2012
dbSNP: rs59065411
rs59065411
1 1.000 0.040 1 156115207 missense variant A/G snv 0.700 1.000 17 1999 2012
dbSNP: rs138592977
rs138592977
3 1.000 0.040 1 156135968 missense variant G/A snv 5.6E-05 6.3E-05 0.010 1.000 1 2012 2012
dbSNP: rs141490569
rs141490569
1 1.000 0.040 1 156136258 missense variant G/A snv 8.0E-05 9.8E-05 0.010 1.000 1 2015 2015
dbSNP: rs760318158
rs760318158
1 1.000 0.040 1 156126897 missense variant C/T snv 2.3E-04 6.3E-05 0.010 1.000 1 2015 2015
dbSNP: rs775964460
rs775964460
1 1.000 0.040 1 156134883 missense variant C/T snv 8.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs1165819867
rs1165819867
1 1.000 0.040 1 156134892 missense variant G/A;T snv 0.700 0
dbSNP: rs1553265180
rs1553265180
1 1.000 0.040 1 156134500 missense variant T/A;G snv 0.700 0
dbSNP: rs1553265736
rs1553265736
4 0.925 0.040 1 156136080 missense variant G/C snv 0.700 0
dbSNP: rs1553265739
rs1553265739
1 1.000 0.040 1 156136081 missense variant A/T snv 0.700 0
dbSNP: rs397517907
rs397517907
2 0.925 0.080 1 156134914 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2015 2015
dbSNP: rs59301204
rs59301204
4 0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 0.010 1.000 1 2017 2017
dbSNP: rs267607581
rs267607581
4 0.925 0.080 1 156137651 splice region variant C/G snv 0.700 0
dbSNP: rs267607578
rs267607578
3 0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 0.810 1.000 24 1999 2014
dbSNP: rs267607570
rs267607570
2 0.925 0.120 1 156130757 missense variant G/A;C snv 4.8E-05 0.800 1.000 20 1999 2017
dbSNP: rs56816490
rs56816490
4 0.925 0.120 1 156135913 stop gained G/A;T snv 0.700 1.000 17 1999 2012
dbSNP: rs59040894
rs59040894
2 0.925 0.120 1 156115184 missense variant G/A;T snv 0.700 1.000 17 1999 2012