Gene: CFHR2 ×
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: rs1853881
rs1853881
CFHR2
1 1.000 0.040 1 196946615 intron variant A/C snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs3828032
rs3828032
CFHR2
1 1.000 0.040 1 196951048 intron variant C/G;T snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs432366
rs432366
CFHR2
1 1.000 0.040 1 196943061 upstream gene variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs9427934
rs9427934
CFHR2
1 1.000 0.040 1 196953730 intron variant G/A snv 0.32 0.700 1.000 1 2013 2013