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: rs1625579
rs1625579
MIR137HG
14 0.763 0.160 1 98037378 intron variant G/T snv 0.78 0.700 1.000 1 2013 2013
dbSNP: rs1782810
rs1782810
MIR137HG
2 1.000 0.040 1 98036784 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs61789073
rs61789073
DPYD ; MIR137HG ; LINC01930
2 1.000 0.040 1 97938540 intron variant T/C snv 4.9E-02 0.700 1.000 1 2017 2017