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: rs57077886
rs57077886
9 0.776 0.240 1 156114947 missense variant C/T 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: rs59040894
rs59040894
2 0.925 0.120 1 156115184 missense variant G/A;T snv 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: rs59065411
rs59065411
1 1.000 0.040 1 156115207 missense variant A/G snv 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: 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: rs61661343
rs61661343
4 0.851 0.040 1 156130687 missense variant T/C snv 0.720 1.000 18 1999 2019
dbSNP: rs28933093
rs28933093
5 0.882 0.160 1 156130741 missense variant G/A snv 0.810 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: rs59026483
rs59026483
7 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.710 0.944 18 1999 2012
dbSNP: rs267607571
rs267607571
4 0.882 0.160 1 156134458 missense variant G/A;T snv 0.700 1.000 17 1999 2012
dbSNP: rs57045855
rs57045855
6 0.882 0.040 1 156134464 missense variant A/G;T snv 0.720 1.000 18 1999 2012
dbSNP: rs28933091
rs28933091
4 0.882 0.160 1 156134474 missense variant C/A;G snv 0.800 1.000 20 1999 2017
dbSNP: rs61195471
rs61195471
6 0.827 0.160 1 156134496 missense variant G/A snv 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: rs1553265180
rs1553265180
1 1.000 0.040 1 156134500 missense variant T/A;G snv 0.700 0
dbSNP: rs267607572
rs267607572
1 1.000 0.040 1 156134518 missense variant T/G snv 0.700 1.000 17 1999 2012
dbSNP: rs61295588
rs61295588
2 0.925 0.160 1 156134809 missense variant T/C snv 0.700 1.000 3 2013 2017
dbSNP: rs58034145
rs58034145
10 0.827 0.160 1 156134830 missense variant A/C snv 0.010 1.000 1 2013 2013
dbSNP: rs60682848
rs60682848
11 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 0.030 1.000 3 2007 2020
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: rs59332535
rs59332535
5 0.827 0.160 1 156134911 missense variant G/A snv 0.700 0