Gene: CCDC162P ×
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: rs1008084
rs1008084
CCDC162P
3 6 109305762 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs11966072
rs11966072
CCDC162P
4 6 109313625 intron variant A/G snv 0.26 0.700 1.000 1 2010 2010
dbSNP: rs13204927
rs13204927
CCDC162P
1 6 109281587 intron variant G/A snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs185030778
rs185030778
CCDC162P
1 6 109277348 intron variant C/T snv 6.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs6568571
rs6568571
CCDC162P
3 6 109292049 intron variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs9386780
rs9386780
CCDC162P
2 6 109263207 intron variant A/G snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs9386791
rs9386791
CCDC162P
2 6 109287294 intron variant C/T snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs9487023
rs9487023
CCDC162P
8 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs9400273
rs9400273
CCDC162P
3 6 109311596 intron variant A/G snv 0.40 0.700 1.000 2 2017 2018