Gene: CPNE4 ×
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: rs1320903
rs1320903
CPNE4
1 3 132039233 intron variant G/A snv 0.31 0.700 1.000 2 2019 2019
dbSNP: rs876424
rs876424
CPNE4
1 3 131918832 intron variant T/G snv 0.40 0.700 1.000 2 2015 2018
dbSNP: rs11925138
rs11925138
CPNE4
1 3 131907204 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs1225051
rs1225051
CPNE4
1 3 131927128 intron variant G/A snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs1225053
rs1225053
CPNE4
1 3 131924008 intron variant T/C snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs7428670
rs7428670
CPNE4 ; LOC105374113
1 3 131860966 intron variant G/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs7631156
rs7631156
CPNE4
1 3 132032784 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs905993
rs905993
CPNE4
1 3 132247903 intron variant G/C snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs9826951
rs9826951
CPNE4
1 3 131719602 intron variant A/G snv 0.75 0.700 1.000 1 2019 2019
dbSNP: rs9856151
rs9856151
CPNE4 ; LOC105374113
1 3 131855641 intron variant G/A snv 0.20 0.700 1.000 1 2015 2015