Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10034228 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 3
rs10089517 0.925 0.040 8 59266162 intergenic variant C/A snv 0.31 2
rs10113215 1.000 0.040 8 59219635 intergenic variant A/G snv 0.33 1
rs10453441
WNT7B
1.000 0.040 22 45967859 intron variant A/G snv 0.40 3
rs10462070
FGF10
1.000 0.040 5 44305647 intron variant A/G snv 1.2E-02 1
rs10488
MMP1 ; WTAPP1
1.000 0.040 11 102797291 synonymous variant C/G;T snv 4.0E-06; 5.7E-02 1
rs104894910
NYX
0.882 0.080 X 41473734 missense variant G/C snv 3
rs10500355
RBFOX1
0.925 0.040 16 7409346 intron variant T/A snv 0.29 3
rs10511652
LOC107986990 ; ADAMTSL1
1.000 0.040 9 18362867 intron variant A/G snv 0.54 1
rs10512441 1.000 0.040 17 32912627 regulatory region variant C/T snv 0.21 1
rs1057518799
POGZ
0.925 0.080 1 151430715 frameshift variant -/GATTGGCA delins 7
rs1057518812
FBN1
0.827 0.240 15 48430742 missense variant T/A snv 6
rs1057518829
CACNA1F
1.000 0.040 X 49230343 stop gained T/A snv 2
rs1057518848
TCF4
0.827 0.240 18 55229003 frameshift variant -/ATTG delins 15
rs1057518881
FBN1
0.827 0.200 15 48513656 missense variant C/A;G;T snv 6
rs1057518891
CHD7
0.851 0.120 8 60854479 stop gained C/T snv 6
rs1057518909
FBN1
0.925 0.120 15 48534099 frameshift variant CATT/- delins 5
rs1057518938
NDE1 ; MYH11
0.882 0.080 16 15724166 missense variant C/G snv 5
rs1064583
NT5DC1 ; COL10A1
0.925 0.040 6 116125413 missense variant A/C;G snv 0.37 2
rs1064795104
EXOC6B
0.790 0.440 2 72498492 stop gained A/C snv 17
rs10824518
KCNMA1
0.882 0.040 10 77303784 intron variant T/A;C snv 3
rs1085307138
PUF60 ; SCRIB
0.807 0.160 8 143817591 splice donor variant C/T snv 9
rs10860860
HELLPAR ; LINC02456
0.925 0.040 12 102387055 non coding transcript exon variant A/T snv 0.28 2
rs10887265
RGR
1.000 0.040 10 84255817 intron variant G/C snv 0.48 1