Gene: ZNF638 ×
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: rs4852252
rs4852252
ZNF638
1 2 71312171 intron variant T/C snv 0.47 0.700 1.000 2 2018 2018
dbSNP: rs12477570
rs12477570
ZNF638
1 2 71281055 intron variant A/C;G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs13035834
rs13035834
ZNF638
1 2 71355123 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1990774
rs1990774
ZNF638
1 2 71341076 intron variant A/G snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs2058898
rs2058898
ZNF638
1 2 71297627 intron variant G/A snv 0.75 0.700 1.000 1 2018 2018
dbSNP: rs2419075
rs2419075
ZNF638
1 2 71307368 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6731420
rs6731420
ZNF638
1 2 71306170 intron variant T/C snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs6745907
rs6745907
ZNF638
1 2 71381943 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs6746731
rs6746731
ZNF638
1 2 71345787 intron variant T/G snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs7557781
rs7557781
ZNF638
2 1.000 0.040 2 71386784 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019