Gene: CFH ×
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: rs10737680
rs10737680
CFH
9 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs10801560
rs10801560
CFH
2 1.000 0.040 1 196745470 intron variant C/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs10801561
rs10801561
CFH
2 1.000 0.040 1 196745540 intron variant T/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs10922106
rs10922106
CFH
4 0.925 0.080 1 196722334 intron variant A/G snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs12041668
rs12041668
CFH
2 1.000 0.040 1 196693917 intron variant C/T snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs12124794
rs12124794
CFH
2 1.000 0.040 1 196692408 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1329428
rs1329428
CFH
9 0.807 0.160 1 196733680 intron variant C/T snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs1410996
rs1410996
CFH
11 0.807 0.240 1 196727803 intron variant G/A snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs1576340
rs1576340
CFH
2 1.000 0.040 1 196729581 intron variant G/T snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs1831281
rs1831281
CFH
2 1.000 0.040 1 196711684 intron variant C/T snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs2284664
rs2284664
CFH
3 0.925 0.040 1 196733395 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs3753395
rs3753395
CFH
5 0.882 0.120 1 196717522 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs529825
rs529825
CFH
2 1.000 0.040 1 196665976 intron variant G/A snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs6680396
rs6680396
CFH
3 1.000 0.040 1 196663340 intron variant A/G snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs7540032
rs7540032
CFH
4 0.925 0.080 1 196732154 intron variant C/T snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs800292
rs800292
CFH
33 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.700 1.000 1 2013 2013