Disease: Myopia
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs866294686
TRIM8 ; LOC105378460
0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs1331463984
TRAF7
0.701 0.240 16 2176350 missense variant G/A snv 33
rs1554208945
ZNF292
0.752 0.240 6 87260207 missense variant A/C snv 26
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 24
rs1064795104
EXOC6B
0.790 0.440 2 72498492 stop gained A/C snv 17
rs397507478
BRAF
0.790 0.440 7 140777014 missense variant C/A snv 12
rs1057518799
POGZ
0.925 0.080 1 151430715 frameshift variant -/GATTGGCA delins 7