Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 7
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 5
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 5
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 4
rs2292910
CRY2
1.000 0.080 11 45882062 3 prime UTR variant A/C snv 0.66 3
rs3736594
MRPL33
2 27772914 intron variant A/C snv 0.62 3
rs143399767 9 93420421 downstream gene variant A/C snv 6.9E-03 1
rs455489
DSCAM
21 40567642 intron variant A/C snv 0.15 1
rs9981885 21 18958319 intron variant A/C snv 0.22 1
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs7867224
GLIS3
9 4292152 intron variant A/C;G snv 0.37 2
rs2018860
IGF1R
0.925 0.120 15 98715481 intron variant A/C;G;T snv 3
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 8
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 5
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 4
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 3
rs6048205
LINC00261
1.000 0.080 20 22578963 upstream gene variant A/G snv 9.1E-02 3
rs7713317
LOC101929710
5 96381018 intron variant A/G snv 0.28 3
rs11041816 11 8222251 downstream gene variant A/G snv 0.36 2
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2