Gene: CFHR4 ×
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: rs1853883
rs1853883
CFHR4 ; LOC105371675
1 1.000 0.040 1 196912470 intron variant G/C;T snv 0.710 1.000 4 2010 2013
dbSNP: rs6685931
rs6685931
CFHR4
2 1.000 0.040 1 196898103 intron variant T/C snv 0.28 0.710 1.000 3 2011 2018
dbSNP: rs1853882
rs1853882
CFHR4 ; LOC105371675
1 1.000 0.040 1 196916214 intron variant C/G snv 0.21 0.700 1.000 2 2010 2013
dbSNP: rs10494745
rs10494745
CFHR4 ; LOC105371675
2 1.000 0.040 1 196918327 missense variant G/A snv 8.0E-02 7.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs10801580
rs10801580
CFHR4 ; LOC105371675
1 1.000 0.040 1 196916555 non coding transcript exon variant T/C snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs10922147
rs10922147
CFHR4
2 1.000 0.040 1 196908559 intron variant C/G snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs1409153
rs1409153
CFHR4 ; LOC105371675
1 1.000 0.040 1 196910875 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1971579
rs1971579
CFHR4 ; LOC105371675
1 1.000 0.040 1 196918051 intron variant T/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs4915559
rs4915559
CFHR4 ; LOC105371675
4 1.000 0.040 1 196917640 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs7366238
rs7366238
CFHR4
2 1.000 0.040 1 196891667 intron variant A/G snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs7525447
rs7525447
CFHR4 ; LOC105371675
1 1.000 0.040 1 196913306 intron variant T/C snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs7533270
rs7533270
CFHR4 ; LOC105371675
1 1.000 0.040 1 196913373 intron variant G/A;T snv 0.700 1.000 1 2013 2013