Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10001410
ADGRL3
1.000 0.040 4 61608511 intron variant C/A snv 0.55 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs104894396
GJB2
0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs10489744
RXRG
0.925 0.040 1 165411386 intron variant G/A snv 0.55 2
rs10492664 0.925 0.040 13 108163877 intergenic variant C/A;T snv 2
rs1049522
SLC1A3
1.000 0.040 5 36686784 3 prime UTR variant A/C snv 0.35 1
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs10514604
ATP2C2
1.000 0.040 16 84412778 intron variant C/A;G snv 1
rs1057517991
MC4R
0.925 0.120 18 60371539 missense variant A/G snv 4.0E-06 2
rs1057518083
DYNC1H1
0.851 0.120 14 101986552 missense variant C/T snv 21
rs1057519438
CDK20
0.925 0.080 9 87969919 stop gained C/G;T snv 4.9E-06 4
rs10762524
PRKG1
1.000 0.040 10 52014152 intron variant T/A;C;G snv 1
rs10823964
PRKG1
1.000 0.040 10 52017283 intron variant T/G snv 0.51 1
rs10823973
PRKG1
1.000 0.040 10 52019720 intron variant C/G;T snv 1
rs10826548 1.000 0.040 10 28966665 intergenic variant C/A snv 0.13 1
rs1085307845
PHIP
0.752 0.320 6 79025582 missense variant G/T snv 21
rs1085308045
PTEN
0.807 0.160 10 87933128 missense variant C/G;T snv 8
rs1085308050
PTEN
0.827 0.160 10 87933178 frameshift variant -/A delins 7
rs1085308056
PTEN
0.851 0.160 10 87957850 splice region variant C/G snv 8
rs10891819
CADM1
1.000 0.040 11 115266527 intron variant T/G snv 0.33 1
rs10910623
MAP10
1.000 0.040 1 232802953 upstream gene variant G/A snv 7.5E-02 1
rs10956838 1.000 0.040 8 92392214 intergenic variant A/C snv 0.28 2
rs10983238
LOC107987015 ; ASTN2
1.000 0.040 9 116571404 intron variant C/A;G snv 0.16 1