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: rs72837826
rs72837826
MIR4435-2HG
1 1.000 0.040 2 111175424 intron variant G/T snv 7.8E-02 0.700 1.000 1 2017 2017