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 0.900 0.893 28 2011 2019
dbSNP: rs2660304
rs2660304
MIR137HG ; MIR137 ; MIR2682
2 0.925 0.120 1 98046571 non coding transcript exon variant G/T snv 0.83 0.710 1.000 3 2015 2018
dbSNP: rs1702294
rs1702294
MIR137HG
1 1.000 0.040 1 98036428 intron variant T/A;C snv 0.700 1.000 3 2014 2019
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
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