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
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
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs7867224
GLIS3
9 4292152 intron variant A/C;G snv 0.37 2
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
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
rs7713317
LOC101929710
5 96381018 intron variant A/G snv 0.28 3
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs2605627
SMCO4
11 93526349 intron variant A/G snv 0.79 2
rs7101470
C11orf49
11 47032897 intron variant A/G snv 7.4E-02 2
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 4
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 5
rs753993
MADD
11 47328418 non coding transcript exon variant C/A snv 0.33 2
rs2302593
SNRPD2 ; QPCTL
19 45693376 intron variant C/A;G snv 1.0E-04; 0.48 2
rs11195502 10 111279909 intergenic variant C/A;G;T snv 2
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14