Gene: CFAP45 ×
Source: GWASDB ×
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: rs10752631
rs10752631
CFAP45
1 1 159892363 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs11265289
rs11265289
CFAP45
1 1 159872313 intron variant C/T snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs11265290
rs11265290
CFAP45
1 1 159873816 intron variant T/C snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs11265291
rs11265291
CFAP45
1 1 159883531 intron variant G/A snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs2494487
rs2494487
CFAP45
1 1 159896670 intron variant A/G snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs3806192
rs3806192
CFAP45 ; MIR4259
1 1 159901394 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs4460634
rs4460634
CFAP45
1 1 159872901 intron variant C/G;T snv 0.67; 4.1E-06 0.700 1.000 1 2011 2011
dbSNP: rs4545332
rs4545332
CFAP45
1 1 159872776 intron variant T/A snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs4656855
rs4656855
CFAP45
1 1 159889470 intron variant T/C snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs4656856
rs4656856
CFAP45
1 1 159889602 intron variant C/T snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs6671929
rs6671929
CFAP45
1 1 159883349 intron variant A/G snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs6682796
rs6682796
CFAP45
1 1 159883032 intron variant G/A;T snv 0.700 1.000 1 2011 2011