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: rs113993396
rs113993396
MIR4435-2HG
1 2 111359727 intron variant C/G snv 5.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs68021656
rs68021656
BCL2L11 ; MIR4435-2HG
1 2 111165509 3 prime UTR variant -/T;TT delins 0.700 1.000 1 2016 2016