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: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 5 132341949 intron variant A/G snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs60978556
rs60978556
SLC22A5 ; MIR3936HG
1 5 132369654 non coding transcript exon variant C/A;G snv 0.700 1.000 1 2019 2019