Source: ALL
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: rs13146355
rs13146355
6 1.000 0.040 4 76490987 intron variant G/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs13191445
rs13191445
4 0.925 0.120 6 26015261 upstream gene variant G/A snv 5.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs1333048
rs1333048
24 0.683 0.320 9 22125348 intron variant A/C snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs13427836
rs13427836
2 1.000 0.040 2 128270387 intron variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs145590578
rs145590578
3 1.000 0.040 6 160236104 intron variant GTT/- delins 9.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs149131600
rs149131600
2 1.000 0.040 19 35058218 intron variant C/A;T snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs1556751
rs1556751
3 1.000 0.040 9 68818296 intron variant G/A snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs16867253
rs16867253
7 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs17137004
rs17137004
2 1.000 0.040 7 114389196 intron variant A/G snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs17140821
rs17140821
16 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918
19 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
16 0.851 0.120 4 139829967 intron variant G/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs1906436
rs1906436
3 1.000 0.040 15 53590245 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs1974990
rs1974990
3 1.000 0.040 2 169790406 non coding transcript exon variant G/T snv 0.90 0.700 1.000 1 2018 2018
dbSNP: rs200950799
rs200950799
3 1.000 0.040 12 17004185 intergenic variant C/T snv 1.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs2023463
rs2023463
3 1.000 0.040 6 29445226 intron variant C/T snv 7.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs2047866
rs2047866
3 1.000 0.040 15 75843853 splice region variant C/T snv 0.54 0.43 0.700 1.000 1 2019 2019
dbSNP: rs2074755
rs2074755
20 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs2079742
rs2079742
9 0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs2105903
rs2105903
3 1.000 0.040 6 32427879 intergenic variant A/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs222826
rs222826
16 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 0.700 1.000 1 2016 2016
dbSNP: rs2421556
rs2421556
3 1.000 0.040 2 73733254 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs247617
rs247617
20 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs2517601
rs2517601
4 0.925 0.080 6 30106295 intron variant G/C snv 0.10 0.700 1.000 1 2019 2019