Gene: MIR29B2CHG ×
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: rs4844392
rs4844392
LOC148696 ; MIR29B2CHG
1 1 207817864 intron variant C/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs4844622
rs4844622
MIR29B2CHG
4 1 207860984 intron variant C/T snv 0.19 0.700 1.000 1 2016 2016