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: rs1048663
rs1048663
CFH
1 1 196705852 intron variant G/A snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs10737680
rs10737680
CFH
9 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs35908703
rs35908703
CFH
1 1 196723810 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs6677604
rs6677604
CFH
7 0.827 0.200 1 196717788 intron variant G/A snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs7517126
rs7517126 		2 1.000 0.040 1 196871142 intron variant A/G snv 0.23 0.700 1.000 1 2017 2017