CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Complement factor H measurement ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1048663
rs1048663 		1 196705852 intron variant G/A snv 0.16
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		0.700 1.000 1 2017 2017
dbSNP: rs10737680
rs10737680 		0.827 0.080 1 196710325 intron variant A/C snv 0.44
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		0.700 1.000 1 2017 2017
dbSNP: rs35908703
rs35908703 		1 196723810 intron variant T/C;G snv
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		0.700 1.000 1 2017 2017
dbSNP: rs6677604
rs6677604 		0.827 0.200 1 196717788 intron variant G/A snv 0.23
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		0.700 1.000 1 2017 2017