Gene: MIR3936HG ×
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: rs12777
rs12777
SLC22A4 ; MIR3936HG
6 5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs270607
rs270607
SLC22A4 ; MIR3936HG
3 5 132313493 intron variant A/G snv 0.69 0.700 1.000 1 2011 2011