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: rs1566816
rs1566816
CEP152
1 1.000 0.040 15 48673021 intergenic variant C/T snv 0.74 0.700 1.000 1 2011 2011
dbSNP: rs1506523
rs1506523
CEP152
1 1.000 0.040 15 48675135 regulatory region variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10851469
rs10851469
CEP152
1 1.000 0.040 15 48676216 intergenic variant C/T snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs10851470
rs10851470
CEP152
1 1.000 0.040 15 48678083 intergenic variant G/A snv 0.69 0.700 1.000 1 2011 2011
dbSNP: rs8038940
rs8038940
CEP152
1 1.000 0.040 15 48681700 regulatory region variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs2045889
rs2045889
CEP152
1 1.000 0.040 15 48692249 intergenic variant T/A snv 0.81 0.700 1.000 1 2011 2011
dbSNP: rs12907144
rs12907144
CEP152
1 1.000 0.040 15 48692625 intergenic variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2045891
rs2045891
CEP152
1 1.000 0.040 15 48695522 regulatory region variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2126905
rs2126905
CEP152
1 1.000 0.040 15 48695847 regulatory region variant C/T snv 0.81 0.700 1.000 1 2011 2011
dbSNP: rs12910178
rs12910178
CEP152
1 1.000 0.040 15 48696754 regulatory region variant C/T snv 0.70 0.700 1.000 1 2011 2011