Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 1
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 1
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 1