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: rs12476527
rs12476527
3 1.000 0.080 2 26692756 5 prime UTR variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13143308
rs13143308
4 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs13299556
rs13299556
1 1.000 0.080 9 26932848 intron variant T/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs13326866
rs13326866
1 1.000 0.080 3 175677201 intron variant A/G snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs138364069
rs138364069
1 1.000 0.080 1 50832533 intron variant C/T snv 1.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs1535459
rs1535459
1 1.000 0.080 9 10550204 intron variant C/G snv 1.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs1570063
rs1570063
1 1.000 0.080 6 49669314 intergenic variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs17490626
rs17490626
5 0.882 0.120 10 69458890 intron variant G/C snv 8.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs17579352
rs17579352
1 1.000 0.080 1 57885133 intron variant C/T snv 2.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs1842681
rs1842681
1 1.000 0.080 18 24761199 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1934066
rs1934066
1 1.000 0.080 1 245508389 intron variant C/T snv 0.85 0.700 1.000 1 2016 2016
dbSNP: rs2005108
rs2005108
3 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2229383
rs2229383
2 1.000 0.080 19 10683954 synonymous variant G/A;C;T snv 4.0E-06; 0.68 0.700 1.000 1 2018 2018
dbSNP: rs2295786
rs2295786
2 1.000 0.080 10 103856724 upstream gene variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs238670
rs238670
2 1.000 0.080 20 23508073 intron variant T/G snv 3.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs2417957
rs2417957
1 1.000 0.080 12 21170677 intron variant C/T snv 9.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs2589998
rs2589998
2 1.000 0.080 7 138181624 intergenic variant C/T snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs2592902
rs2592902
2 1.000 0.080 1 159685936 intergenic variant G/A;T snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs2634074
rs2634074
1 1.000 0.080 4 110755885 intergenic variant T/A snv 0.66 0.700 1.000 1 2016 2016
dbSNP: rs2801231
rs2801231
2 1.000 0.080 X 122083259 intergenic variant T/A;C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs2825226
rs2825226
1 1.000 0.080 21 18909856 intergenic variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs3176471
rs3176471
1 1.000 0.080 1 50973784 intron variant A/T snv 1.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs3184504
rs3184504
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs34234989
rs34234989
5 0.882 0.120 20 35186731 intron variant A/- delins 0.40 0.700 1.000 1 2016 2016
dbSNP: rs34311906
rs34311906
2 1.000 0.080 4 112810934 intergenic variant T/C snv 0.43 0.700 1.000 1 2018 2018