Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800012
COL1A1
0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs1800255
COL3A1
0.851 0.160 2 188999354 missense variant G/A snv 0.25 0.21 5
rs4662344
ARHGAP15
0.925 0.080 2 143591289 intron variant T/C snv 0.82 3
rs7609897
COLQ
0.925 0.080 3 15461174 intron variant G/T snv 0.22 3
rs67153654
FAM155A
0.925 0.080 13 107572636 intron variant T/A;C snv 3
rs3134646 0.925 0.080 2 189015117 downstream gene variant G/A snv 0.41 2