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: rs3806932
rs3806932
3 0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 0.720 1.000 2 2010 2015
dbSNP: rs11206830
rs11206830
1 1.000 0.120 1 56494451 intron variant C/T snv 8.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs11495981
rs11495981
2 1.000 0.120 7 28137682 intron variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs118086209
rs118086209
1 1.000 0.120 11 86393453 intron variant T/C;G snv 0.700 1.000 1 2014 2014
dbSNP: rs11819199
rs11819199
1 1.000 0.120 10 20576228 intergenic variant A/G snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs12924112
rs12924112
1 1.000 0.120 16 11125863 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs149864795
rs149864795
1 1.000 0.120 2 31179541 intron variant G/A snv 4.8E-02 0.700 1.000 1 2014 2014
dbSNP: rs167769
rs167769
5 0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs17004598
rs17004598
1 1.000 0.120 21 43658675 intron variant T/G snv 4.5E-02 0.700 1.000 1 2014 2014
dbSNP: rs1986734
rs1986734
3 1.000 0.120 4 76499631 intron variant C/T snv 0.43 0.700 1.000 1 2010 2010
dbSNP: rs2000260
rs2000260
1 1.000 0.120 1 108130783 downstream gene variant A/G snv 0.37 0.700 1.000 1 2014 2014
dbSNP: rs2055376
rs2055376
1 1.000 0.120 5 116845732 regulatory region variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs2075277
rs2075277
1 1.000 0.120 22 21028193 3 prime UTR variant T/C snv 0.19 0.700 1.000 1 2014 2014
dbSNP: rs2155219
rs2155219
14 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 0.700 1.000 1 2014 2014
dbSNP: rs2296225
rs2296225
3 0.882 0.160 1 20704549 missense variant T/C;G snv 0.12; 4.0E-06 0.700 1.000 1 2014 2014
dbSNP: rs252716
rs252716
1 1.000 0.120 5 111089365 intron variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs28530674
rs28530674
1 1.000 0.120 1 18907640 3 prime UTR variant A/G snv 0.11 0.700 1.000 1 2014 2014
dbSNP: rs2898261
rs2898261
1 1.000 0.120 8 11101029 intron variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs371915
rs371915
1 1.000 0.120 16 84544635 intron variant A/C;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs3744790
rs3744790
1 1.000 0.120 17 78897053 intron variant C/T snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs3806933
rs3806933
7 0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 0.700 1.000 1 2014 2014
dbSNP: rs3815700
rs3815700
1 1.000 0.120 19 32602346 intron variant T/C snv 0.19 0.700 1.000 1 2014 2014
dbSNP: rs4240384
rs4240384
1 1.000 0.120 5 124955709 intron variant T/C snv 0.85 0.700 1.000 1 2019 2019
dbSNP: rs599707
rs599707
2 0.925 0.200 6 31840659 downstream gene variant C/T snv 7.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs61894547
rs61894547
4 0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 0.700 1.000 1 2014 2014