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: rs7523273
rs7523273
MIR29B2 ; MIR29C ; MIR29B2CHG
1 1.000 0.040 1 207803738 non coding transcript exon variant A/G snv 0.30 0.700 1.000 5 2014 2019
dbSNP: rs10863593
rs10863593
MIR29B2CHG
1 1.000 0.040 1 207844729 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018