Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs1408272
SLC17A3
6 25842723 intron variant T/G snv 4.0E-02 4
rs10047462
APOA1-AS ; SIK3
11 116851325 intron variant G/C;T snv 3
rs7940310
PAFAH1B2
11 117153765 intron variant T/A;C snv 3
rs1242229
SIDT2
11 117191654 non coding transcript exon variant T/A;C;G snv 2
rs7112513
PAFAH1B2
11 117166645 intron variant A/G snv 0.85 1