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: rs7009139
rs7009139
CCDC26
1 1.000 0.080 8 128902002 intron variant G/A snv 0.46 0.700 1.000 1 2009 2009
dbSNP: rs7015145
rs7015145
CCDC26
1 1.000 0.080 8 128697039 intron variant A/G snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs7018275
rs7018275
CCDC26
1 1.000 0.080 8 129004253 intron variant C/T snv 0.90 0.700 1.000 1 2012 2012
dbSNP: rs72728734
rs72728734
CCDC26
3 0.882 0.120 8 128921474 intron variant A/G snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs7460492
rs7460492
CCDC26
1 1.000 0.080 8 128779681 intron variant G/A snv 0.32 0.700 1.000 1 2009 2009
dbSNP: rs748978
rs748978
CCDC26
1 1.000 0.080 8 128990870 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs766812
rs766812
CCDC26
1 1.000 0.080 8 128992458 intron variant A/G snv 0.91 0.700 1.000 1 2009 2009
dbSNP: rs7815713
rs7815713
CCDC26
1 1.000 0.080 8 128883227 intron variant T/C snv 0.69 0.700 1.000 1 2009 2009
dbSNP: rs7822386
rs7822386
CCDC26
1 1.000 0.080 8 129212475 intron variant A/G snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs7826130
rs7826130
CCDC26
1 1.000 0.080 8 129212496 intron variant C/T snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs7826294
rs7826294
CCDC26
1 1.000 0.080 8 129212646 intron variant C/T snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs7826688
rs7826688
CCDC26
1 1.000 0.080 8 129212765 intron variant G/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs7835741
rs7835741
CCDC26
1 1.000 0.080 8 129005468 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs7838330
rs7838330
CCDC26
1 1.000 0.080 8 128980860 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs9297775
rs9297775
CCDC26
1 1.000 0.080 8 128724466 intron variant C/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs997310
rs997310
CCDC26
1 1.000 0.080 8 128908034 intron variant C/A;G;T snv 0.700 1.000 1 2009 2009