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: rs17114036
rs17114036
5 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.710 1.000 3 2013 2018
dbSNP: rs17114046
rs17114046
2 0.925 0.040 1 56500678 intron variant A/G snv 0.12 0.700 1.000 2 2018 2018
dbSNP: rs147055617
rs147055617
1 1.000 0.040 1 56520631 intron variant A/G snv 8.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs17416285
rs17416285
1 1.000 0.040 1 56554977 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4634932
rs4634932
1 1.000 0.040 1 56530519 intron variant T/C snv 7.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs56170783
rs56170783
1 1.000 0.040 1 56550459 intron variant A/C snv 6.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs9970807
rs9970807
2 0.925 0.080 1 56499992 intron variant C/T snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs72664324
rs72664324
2 1.000 0.040 1 56506681 intron variant G/A snv 0.10 0.010 1.000 1 2015 2015