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: rs147858478
rs147858478
MIR3936HG
1 5 132347093 intron variant GAGTTCT/-;GAGTTCTGAGTTCT delins 0.700 1.000 1 2016 2016
dbSNP: rs538021413
rs538021413
SLC22A4 ; MIR3936HG
1 5 132328824 intron variant TATATATATATA/-;TA;TATA;TATATA;TATATATA;TATATATATA;TATATATATATATA;TATATATATATATATA delins 0.39 0.700 1.000 1 2016 2016