Gene: ACOXL ×
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: rs150449635
rs150449635
ACOXL
2 2 110994574 intron variant T/C snv 1.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs2062225
rs2062225
ACOXL
2 2 110993295 intron variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3789087
rs3789087
ACOXL ; MIR4435-2HG
2 2 111034076 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs3789088
rs3789088
ACOXL ; MIR4435-2HG
2 2 111033227 intron variant G/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs7578982
rs7578982
ACOXL ; MIR4435-2HG
4 2 111078961 intron variant T/C snv 0.27 0.700 1.000 1 2011 2011