Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs243080
MIR4432 ; MIR4432HG
2 60387437 non coding transcript exon variant G/A snv 0.48 0.41 3
rs243078
MIR4432 ; MIR4432HG
2 60388168 intron variant A/G snv 0.42 2
rs243079
MIR4432HG ; MIR4432
2 60387893 intron variant A/C snv 0.42 2