Gene: MIR5196 ×
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: rs10406069
rs10406069
CD22 ; MIR5196
1 1.000 0.040 19 35345627 missense variant G/A;C snv 0.16 0.010 1.000 1 2012 2012
dbSNP: rs10413500
rs10413500
CD22 ; MIR5196
1 1.000 0.040 19 35345923 intron variant C/G snv 0.16 0.010 1.000 1 2012 2012
dbSNP: rs34826052
rs34826052
CD22 ; MIR5196
1 1.000 0.040 19 35345697 synonymous variant C/A;T snv 4.0E-02; 7.6E-05 0.010 1.000 1 2012 2012