Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1232880706
FBN1
0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs137854539
GNAS
0.716 0.520 20 58903703 missense variant C/T snv 28
rs398122394
ALG13
0.763 0.240 X 111685040 missense variant A/G snv 17
rs875989883
PTCHD1-AS ; PHEX
0.851 0.280 X 22219070 missense variant G/A;C snv 9
rs104894347
FGF23
0.925 0.200 12 4370572 missense variant C/T snv 7.0E-06 3