Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397515453
PIK3R1
0.752 0.440 5 68296301 missense variant C/T snv 3
rs397514487
POC1A
0.882 0.200 3 52149850 stop gained G/A snv 7.0E-06 3
rs121912889
COL2A1
0.851 0.160 12 47974234 missense variant T/C snv 2
rs121917883
GHSR
0.851 0.160 3 172447803 missense variant G/A;T snv 2.8E-05 2
rs60310264
LMNA
0.827 0.200 1 156130693 missense variant G/A snv 2
rs397514461
SHOX
0.827 0.200 Y 640842 missense variant G/C snv 2
rs387906918
CDT1
0.925 0.120 16 88804027 missense variant G/A snv 7.0E-06 1
rs137853221
CSHL1 ; GH1 ; LOC112268204
0.925 0.160 17 63917803 missense variant T/C snv 1
rs75790268
FGFR3
0.925 0.120 4 1804377 missense variant G/T snv 1
rs80053154
FGFR3
0.925 0.120 4 1805636 missense variant A/G snv 1.2E-05 7.0E-06 1
rs121909362
GHR
0.827 0.160 5 42699919 missense variant C/T snv 3.9E-03 4.1E-03 1
rs886037910
GHR
0.925 0.160 5 42699943 missense variant T/C snv 1
rs137853223
LOC112268204 ; CSHL1 ; GH1
0.851 0.160 17 63917337 missense variant C/T snv 7.0E-06 1
rs137853220
LOC112268204 ; GH1 ; CSHL1
0.882 0.200 17 63917909 missense variant G/A snv 4.0E-06 1
rs137853222
LOC112268204 ; GH1 ; CSHL1
0.925 0.160 17 63918072 missense variant C/A;G snv 1
rs111033552
NT5DC1 ; COL10A1
0.925 0.120 6 116120105 missense variant A/G snv 1
rs121917843
PROP1
0.882 0.160 5 177994231 missense variant G/A snv 4.0E-06 1
rs2076739
TG
0.827 0.200 8 132971804 missense variant T/A snv 1
rs1555545033
THRA
0.807 0.160 17 40088306 missense variant C/T snv 1
rs137853092
WNK4
0.851 0.240 17 42787494 missense variant C/G snv 1