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: rs200980971
rs200980971
CCDC162P
2 6 109261139 intron variant A/-;AA delins 0.700 1.000 1 2017 2017
dbSNP: rs36052053
rs36052053
CCDC162P
2 6 109262596 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs6568570
rs6568570
CCDC162P
2 6 109292038 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs9480924
rs9480924
CCDC162P
2 6 109295867 intron variant T/C snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs9487023
rs9487023
CCDC162P
8 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2017 2017