Gene: CCDC170 ×
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: rs1038304
rs1038304
CCDC170 ; LOC107986528
4 0.882 0.160 6 151612040 intron variant A/G snv 0.58 0.800 1.000 3 2008 2009
dbSNP: rs4870044
rs4870044
CCDC170
3 1.000 0.080 6 151580274 intron variant C/T snv 0.44 0.800 1.000 3 2008 2009
dbSNP: rs4869742
rs4869742
CCDC170
2 6 151586613 intron variant C/A;G;T snv 0.800 1.000 2 2009 2012
dbSNP: rs6909279
rs6909279
CCDC170
2 6 151574321 intron variant G/C;T snv 0.800 1.000 2 2009 2013
dbSNP: rs6929137
rs6929137
CCDC170 ; LOC107986528
6 0.851 0.160 6 151615542 missense variant G/A snv 0.31 0.36 0.800 1.000 2 2009 2009
dbSNP: rs7753676
rs7753676
CCDC170
1 6 151555680 intron variant G/A snv 0.48 0.700 1.000 2 2009 2009
dbSNP: rs1023940
rs1023940
CCDC170 ; LOC107986528
1 6 151611643 intron variant A/G snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs11155797
rs11155797
CCDC170
1 6 151580202 intron variant C/T snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs12197879
rs12197879
CCDC170
1 6 151574642 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1871859
rs1871859
CCDC170
2 6 151577371 intron variant C/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs3734804
rs3734804
CCDC170 ; LOC107986528
1 6 151618046 missense variant G/A snv 0.49 0.57 0.700 1.000 1 2009 2009
dbSNP: rs3734806
rs3734806
CCDC170
1 6 151620326 3 prime UTR variant G/A snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs3757322
rs3757322
CCDC170
2 1.000 0.080 6 151621059 3 prime UTR variant T/G snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs4869739
rs4869739
CCDC170
2 1.000 0.080 6 151580667 intron variant A/T snv 0.44 0.700 1.000 1 2009 2009
dbSNP: rs4869741
rs4869741
CCDC170
1 6 151585158 intron variant T/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs6557155
rs6557155
CCDC170
1 6 151588991 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs6931664
rs6931664
CCDC170
1 6 151536459 intron variant A/C;G snv 4.0E-06; 0.51 0.700 1.000 1 2009 2009
dbSNP: rs6932260
rs6932260
CCDC170 ; LOC107986528
1 6 151618425 3 prime UTR variant T/C snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs6932603
rs6932603
CCDC170 ; LOC107986528
1 6 151618635 3 prime UTR variant T/C snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs7761420
rs7761420
CCDC170
1 6 151551432 intron variant C/T snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs9383929
rs9383929
CCDC170
1 6 151590737 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs9478217
rs9478217
CCDC170
1 6 151552987 intron variant A/G snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs9479055
rs9479055
CCDC170
1 6 151526832 intron variant C/A snv 0.46 0.700 1.000 1 2009 2009
dbSNP: rs9479068
rs9479068
CCDC170
1 6 151551313 intron variant G/T snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs9479072
rs9479072
CCDC170
1 6 151569654 intron variant C/T snv 0.43 0.700 1.000 1 2009 2009