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: rs1192415
rs1192415
4 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 0.700 1.000 2 2019 2019
dbSNP: rs17009288
rs17009288
2 1 221030957 regulatory region variant A/C snv 0.30 0.700 1.000 2 2019 2019
dbSNP: rs35043843
rs35043843
3 1 118368672 intergenic variant T/G snv 0.21 0.700 1.000 2 2019 2019
dbSNP: rs878471
rs878471
2 1 150575271 3 prime UTR variant G/A snv 0.48 0.700 1.000 2 2019 2019
dbSNP: rs1008833
rs1008833
3 1 204457167 intron variant A/G snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs10157038
rs10157038
1 1 10652408 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1046874
rs1046874
1 1 204557932 3 prime UTR variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs10737680
rs10737680
CFH
9 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs10779447
rs10779447
1 1 221587993 intergenic variant A/G snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs10914269
rs10914269
1 1 31096384 upstream gene variant G/T snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs10917165
rs10917165
1 1 22175135 intergenic variant T/C snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs111962736
rs111962736
1 1 118739138 regulatory region variant A/G snv 4.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs11208662
rs11208662
1 1 65521481 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11209152
rs11209152
1 1 67802624 intron variant C/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs11260629
rs11260629
1 1 1774506 intron variant T/C snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs11264341
rs11264341
4 0.925 0.120 1 155179017 intron variant C/T snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs115979533
rs115979533
1 1 21939837 upstream gene variant C/G snv 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs12046746
rs12046746
1 1 221461865 intergenic variant C/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs12096239
rs12096239
3 1 26470431 3 prime UTR variant G/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs12128356
rs12128356
1 1 22331992 intergenic variant G/A snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs12131063
rs12131063
1 1 150195892 intergenic variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs12141189
rs12141189
1 1 220880203 missense variant T/C snv 0.24 0.23 0.700 1.000 1 2019 2019
dbSNP: rs12724426
rs12724426
1 1 147022468 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12737805
rs12737805
2 1 22286197 regulatory region variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs12746703
rs12746703
1 1 82751708 intron variant T/C snv 0.27 0.700 1.000 1 2019 2019