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: rs1991866
rs1991866
CCDC26
3 8 129611859 intron variant G/A;C snv 0.700 1.000 2 2014 2017
dbSNP: rs10098310
rs10098310
CCDC26
3 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10956483
rs10956483
CCDC26
3 8 129559864 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11327184
rs11327184
CCDC26
4 8 129592027 intron variant C/- delins 0.40 0.700 1.000 1 2016 2016
dbSNP: rs13277237
rs13277237
CCDC26
4 8 129592317 intron variant G/A snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs138628047
rs138628047
CCDC26
2 8 129666460 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs35389394
rs35389394
CCDC26
2 8 129609008 intron variant C/T snv 0.56 0.700 1.000 1 2018 2018