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: rs9895661
rs9895661
10 0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 0.700 1.000 9 2016 2019
dbSNP: rs77924615
rs77924615
7 1.000 0.080 16 20381010 intron variant G/A snv 0.16 0.700 1.000 7 2016 2019
dbSNP: rs963837
rs963837
8 0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 0.700 1.000 7 2016 2019
dbSNP: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 6 2013 2019
dbSNP: rs62435145
rs62435145
8 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 0.700 1.000 6 2016 2019
dbSNP: rs881858
rs881858
7 0.882 0.200 6 43838872 intron variant G/A;C snv 0.700 1.000 6 2016 2019
dbSNP: rs1047891
rs1047891
34 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 0.700 1.000 5 2017 2019
dbSNP: rs11123169
rs11123169
3 1.000 0.080 2 113209498 upstream gene variant C/A;T snv 0.700 1.000 5 2018 2019
dbSNP: rs12509595
rs12509595
10 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 0.700 1.000 5 2018 2019
dbSNP: rs17216707
rs17216707
6 20 54115823 intergenic variant T/C snv 0.17 0.700 1.000 5 2016 2019
dbSNP: rs2279463
rs2279463
4 1.000 0.080 6 160247357 intron variant A/G;T snv 0.700 1.000 5 2016 2019
dbSNP: rs3850625
rs3850625
3 1 201047168 missense variant G/A snv 0.12 8.9E-02 0.700 1.000 5 2016 2019
dbSNP: rs80282103
rs80282103
4 1.000 0.080 10 853131 intron variant A/T snv 0.12 0.700 1.000 5 2017 2019
dbSNP: rs8096658
rs8096658
5 0.925 0.120 18 79396537 intron variant C/G snv 0.39 0.700 1.000 5 2016 2019
dbSNP: rs10851885
rs10851885
5 0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18 0.700 1.000 4 2017 2019
dbSNP: rs1275609
rs1275609
3 12 75877403 intron variant G/A snv 0.40 0.700 1.000 4 2018 2019
dbSNP: rs16942751
rs16942751
3 1.000 0.080 18 26813249 intron variant C/A;T snv 0.700 1.000 4 2018 2019
dbSNP: rs2039424
rs2039424
2 1.000 0.080 9 68817258 intron variant G/A snv 0.63 0.700 1.000 4 2019 2019
dbSNP: rs267738
rs267738
4 1.000 0.040 1 150968149 missense variant T/A;G snv 4.0E-06; 0.15 0.700 1.000 4 2017 2019
dbSNP: rs3812036
rs3812036
5 0.925 0.120 5 177386403 intron variant C/T snv 0.23 0.20 0.700 1.000 4 2017 2019
dbSNP: rs6971211
rs6971211
2 7 155871992 intergenic variant C/A;T snv 0.40 0.700 1.000 4 2017 2019
dbSNP: rs10265221
rs10265221
3 7 151717243 intron variant T/A;C snv 0.700 1.000 3 2016 2019
dbSNP: rs10994856
rs10994856
5 0.925 0.120 10 50885488 intron variant G/A snv 0.19 0.700 1.000 3 2017 2019
dbSNP: rs113246091
rs113246091
2 5 68443447 regulatory region variant G/A;T snv 8.7E-02 0.700 1.000 3 2017 2019
dbSNP: rs12722725
rs12722725
1 1 112716059 non coding transcript exon variant T/C snv 8.9E-02 0.700 1.000 3 2019 2019