Gene: CCDC26 ×
Source: INFERRED ×
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: rs10098310
rs10098310
CCDC26
3 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1433578
rs1433578
CCDC26
1 8 129588843 intron variant T/C snv 9.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs1982094
rs1982094
CCDC26
5 8 129612570 intron variant C/T snv 4.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs2163950
rs2163950
CCDC26
1 8 129585339 intron variant C/A snv 9.2E-02 0.700 1.000 1 2014 2014
dbSNP: rs397731840
rs397731840
CCDC26
5 8 129599504 intron variant TT/-;T;TTT;TTTT;TTTTT delins 0.700 1.000 1 2016 2016
dbSNP: rs55964818
rs55964818
CCDC26
1 8 129593625 intron variant T/C snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs9297779
rs9297779
CCDC26
1 8 128973991 intron variant C/G;T snv 0.700 1.000 1 2019 2019