Gene: MIR4435-2HG ×
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: 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: rs6734942
rs6734942
BCL2L11 ; MIR4435-2HG
2 2 111153117 intron variant C/G;T snv 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