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: rs10836347
rs10836347
3 1.000 0.080 11 35231586 3 prime UTR variant C/T snv 0.11 0.010 < 0.001 1 2016 2016
dbSNP: rs11821102
rs11821102
2 11 35230997 3 prime UTR variant G/A snv 6.8E-02 0.020 1.000 2 2016 2016
dbSNP: rs13347
rs13347
12 0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 0.030 1.000 3 2016 2016
dbSNP: rs187115
rs187115
22 0.695 0.320 11 35154612 intron variant T/C snv 0.37 0.040 0.750 4 2016 2019
dbSNP: rs713330
rs713330
3 1.000 0.040 11 35202398 intron variant C/T snv 0.74 0.020 < 0.001 2 2016 2016
dbSNP: rs751144688
rs751144688
4 1.000 0.080 11 35206195 missense variant C/T snv 4.0E-06 0.010 1.000 1 2020 2020
dbSNP: rs8193
rs8193
4 0.925 0.080 11 35229771 3 prime UTR variant C/T snv 0.29 0.010 1.000 1 2020 2020