Gene: BCL2L11 ×
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: rs11691517
rs11691517
BCL2L11 ; MIR4435-2HG
1 1.000 0.080 2 111135519 intron variant T/G snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs56366063
rs56366063
BCL2L11 ; MIR4435-2HG
1 1.000 0.080 2 111146954 intron variant C/A snv 7.2E-02 0.700 1.000 1 2018 2018