Gene: MIR137HG ×
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: rs9324380
rs9324380
MIR137HG
1 1 97995576 intron variant G/C snv 0.91 0.700 1.000 2 2018 2019
dbSNP: rs11804556
rs11804556
MIR137HG
1 1 98032885 intron variant G/A snv 6.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs190925241
rs190925241
MIR137HG
1 1 98035093 intron variant T/A snv 8.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs80289781
rs80289781
DPYD ; MIR137HG
2 1.000 0.040 1 97980274 intron variant C/G;T snv 0.700 1.000 1 2019 2019