Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs374823079
MFRP ; C1QTNF5
1.000 0.080 11 119341673 missense variant G/A snv 8.5E-05 3.5E-05 1
rs387907095
PRSS56
0.925 0.080 2 232523492 missense variant G/C snv 1
rs587777690
TMEM98
0.925 0.080 17 32940889 missense variant G/C;T snv 4.0E-06 1
rs869312733
TMEM98
0.925 0.080 17 32940899 missense variant A/C snv 1
rs387907252
VAX1
0.882 0.160 10 117134559 missense variant G/T snv 1
rs755799430
VSX2
0.925 0.080 14 74259689 missense variant G/A snv 8.0E-06 1.4E-05 1
rs869025268
VSX2
1.000 0.080 14 74239626 frameshift variant -/G delins 1.3E-05 1
rs1475762618
WNT7B
1.000 0.080 22 45923167 missense variant G/A snv 1