Gene: CCDC26 ×
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: rs1030608
rs1030608
CCDC26
1 1.000 0.080 8 128727506 intron variant G/A snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs1030609
rs1030609
CCDC26
1 1.000 0.080 8 128727631 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs10808576
rs10808576
CCDC26
1 1.000 0.080 8 129051725 intron variant T/G snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs10956453
rs10956453
CCDC26
1 1.000 0.080 8 128937545 intron variant G/C snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs11506137
rs11506137
CCDC26
1 1.000 0.080 8 128916902 non coding transcript exon variant C/T snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs1155582
rs1155582
CCDC26
1 1.000 0.080 8 128882775 intron variant C/G snv 0.64 0.700 1.000 1 2009 2009
dbSNP: rs11989880
rs11989880
CCDC26
1 1.000 0.080 8 128860736 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs11994831
rs11994831
CCDC26
1 1.000 0.080 8 128876235 intron variant C/T snv 0.52 0.700 1.000 1 2009 2009
dbSNP: rs11996876
rs11996876
CCDC26
1 1.000 0.080 8 129074926 intron variant T/C snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs12334809
rs12334809
CCDC26
1 1.000 0.080 8 129018760 non coding transcript exon variant T/C snv 0.88 0.700 1.000 1 2012 2012
dbSNP: rs12546244
rs12546244
CCDC26 ; LINC00976
1 1.000 0.080 8 128958000 intron variant G/A snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs13265167
rs13265167
CCDC26
1 1.000 0.080 8 128947070 intron variant C/T snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs13274247
rs13274247
CCDC26
1 1.000 0.080 8 128969222 intron variant G/A snv 0.38 0.700 1.000 1 2009 2009
dbSNP: rs1372449
rs1372449
CCDC26
1 1.000 0.080 8 128938144 intron variant G/A snv 0.32 0.700 1.000 1 2009 2009
dbSNP: rs1372452
rs1372452
CCDC26
1 1.000 0.080 8 129016788 intron variant A/G snv 0.90 0.700 1.000 1 2012 2012
dbSNP: rs1432017
rs1432017
CCDC26
1 1.000 0.080 8 128723840 intron variant C/T snv 0.32 0.700 1.000 1 2009 2009
dbSNP: rs1441994
rs1441994
CCDC26 ; LINC00976
1 1.000 0.080 8 128956941 intron variant T/C snv 0.32 0.700 1.000 1 2009 2009
dbSNP: rs17241253
rs17241253
CCDC26
1 1.000 0.080 8 128877942 intron variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs17820135
rs17820135
CCDC26
1 1.000 0.080 8 128935540 intron variant T/G snv 6.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs17821251
rs17821251
CCDC26
1 1.000 0.080 8 128996987 intron variant T/C snv 6.3E-02 0.700 1.000 1 2009 2009
dbSNP: rs2197111
rs2197111
CCDC26
1 1.000 0.080 8 129003469 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs3857888
rs3857888
CCDC26
1 1.000 0.080 8 128812615 intron variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs3935421
rs3935421
CCDC26
1 1.000 0.080 8 129190893 intron variant A/G snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs4422741
rs4422741
CCDC26
1 1.000 0.080 8 129199082 intron variant T/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs4472475
rs4472475
CCDC26
1 1.000 0.080 8 129209789 intron variant A/G snv 0.13 0.700 1.000 1 2009 2009