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: rs1057515421
rs1057515421
2 0.925 0.120 1 156136284 stop gained C/T snv 0.700 1.000 2 1999 2016
dbSNP: rs11575937
rs11575937
29 0.653 0.480 1 156136985 missense variant G/A;T snv 0.700 0
dbSNP: rs1165819867
rs1165819867
1 1.000 0.040 1 156134892 missense variant G/A;T snv 0.700 0
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: rs142000963
rs142000963
8 0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 0.010 1.000 1 2012 2012
dbSNP: rs150840924
rs150840924
7 0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 0.700 1.000 17 1999 2012
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: 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: 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: rs267607571
rs267607571
4 0.882 0.160 1 156134458 missense variant G/A;T snv 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: rs267607576
rs267607576
2 0.925 0.160 1 156136219 missense variant G/A;C snv 1.2E-05 0.700 1.000 17 1999 2012
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: rs267607581
rs267607581
4 0.925 0.080 1 156137651 splice region variant C/G snv 0.700 0
dbSNP: rs28928900
rs28928900
2 0.925 0.120 1 156115096 missense variant C/G;T snv 0.800 0
dbSNP: rs28933090
rs28933090
3 0.925 0.160 1 156115172 missense variant T/A;G snv 0.800 1.000 20 1999 2017
dbSNP: rs28933091
rs28933091
4 0.882 0.160 1 156134474 missense variant C/A;G snv 0.800 1.000 20 1999 2017
dbSNP: rs28933092
rs28933092
2 1.000 0.040 1 156134497 missense variant A/G;T snv 0.800 1.000 17 1999 2012
dbSNP: rs28933093
rs28933093
5 0.882 0.160 1 156130741 missense variant G/A snv 0.810 1.000 17 1999 2012