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: rs932223
rs932223
CCDC162P
2 6 109265453 intron variant T/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs9374081
rs9374081
CCDC162P
2 6 109310579 intron variant A/G snv 0.26 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 2016 2016
dbSNP: rs9487051
rs9487051
CCDC162P
1 6 109295876 intron variant A/G snv 0.41 0.700 1.000 1 2016 2016