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: rs672601334
rs672601334
18 0.752 0.400 1 155904798 missense variant G/C snv 0.710 1.000 7 2013 2019
dbSNP: rs869025194
rs869025194
4 0.882 0.280 1 155904496 missense variant A/C;G;T snv 0.710 1.000 1 2016 2016
dbSNP: rs483352822
rs483352822
16 0.776 0.360 1 155904470 stop lost C/A;G;T snv 0.700 1.000 7 2013 2016
dbSNP: rs869025189
rs869025189
2 0.925 0.160 1 155910658 missense variant C/G snv 7.0E-06 0.700 1.000 5 2013 2016
dbSNP: rs672601335
rs672601335
3 0.882 0.160 1 155904456 missense variant C/G snv 0.700 1.000 4 2013 2014
dbSNP: rs869025191
rs869025191
9 0.827 0.160 1 155904739 missense variant C/A;G;T snv 0.700 1.000 3 2014 2016
dbSNP: rs869025193
rs869025193
2 0.925 0.160 1 155904498 missense variant T/C snv 0.700 1.000 3 2013 2016
dbSNP: rs869025196
rs869025196
1 1.000 0.160 1 155904489 missense variant G/A snv 7.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs730881014
rs730881014
15 0.776 0.360 1 155904494 stop gained A/C;G;T snv 0.700 0
dbSNP: rs869025190
rs869025190
1 1.000 0.160 1 155910462 missense variant C/A snv 0.700 0
dbSNP: rs869025192
rs869025192
1 1.000 0.160 1 155904499 missense variant C/G snv 0.700 0
dbSNP: rs869025195
rs869025195
11 0.790 0.280 1 155904493 missense variant T/G snv 0.700 0
dbSNP: rs869025197
rs869025197
2 0.925 0.160 1 155904475 missense variant A/G snv 0.700 0