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: rs646776
rs646776
25 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.800 1.000 4 2012 2019
dbSNP: rs629301
rs629301
22 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 0.800 1.000 3 2012 2018
dbSNP: rs7528419
rs7528419
13 0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 0.800 1.000 3 2012 2019
dbSNP: rs12740374
rs12740374
16 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.800 1.000 2 2012 2018
dbSNP: rs6657811
rs6657811
4 1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 0.700 1.000 2 2015 2018
dbSNP: rs3832016
rs3832016
4 1 109275536 3 prime UTR variant -/T ins 0.74 0.700 1.000 1 2018 2018
dbSNP: rs4970834
rs4970834
8 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.700 1.000 1 2012 2012
dbSNP: rs660240
rs660240
6 1 109275216 3 prime UTR variant T/C snv 0.75 0.700 1.000 1 2018 2018