Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs1800472
TGFB1
0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 11
rs11327935
COL1A1
1.000 0.040 17 50203295 intron variant AA/-;A;AAA delins 0.18 2
rs39399
RELN
0.925 0.040 7 103849545 intron variant G/A;T snv 2
rs1352713791
BMP4 ; MIR5580
1.000 0.040 14 53950282 missense variant A/G snv 7.0E-06 1
rs3914132
RELN
1.000 0.040 7 103886922 intron variant C/A;T snv 1
rs39335
RELN
1.000 0.040 7 103813122 intron variant T/C snv 0.21 1
rs1323853167
TNFSF11
1.000 0.040 13 42574312 synonymous variant C/G snv 1
rs1234261
ZNF383
1.000 0.040 19 37230070 intron variant C/A;T snv 0.18 1