Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10513801
ETV5
3 186104564 intron variant T/G snv 9.2E-02 3
rs10874312 1 82478888 intron variant G/A snv 0.70 3
rs112545201
ETV5
3 186085743 intron variant C/T snv 0.14 3
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 3
rs12428035 13 95648618 upstream gene variant C/A;T snv 3
rs1275609
LOC105369844
12 75877403 intron variant G/A snv 0.40 3
rs143193096
IGF1R
15 98916098 missense variant G/A;C snv 8.4E-05; 4.0E-06 3
rs151134704
NFKB1 ; LOC105377347
4 102616435 splice region variant C/T snv 1.6E-04 9.1E-05 3
rs16856823
LRP2
2 169343942 intron variant A/T snv 4.6E-02 3
rs199592697
WNT7A
3 13854632 missense variant C/T snv 1.7E-04 1.1E-04 3
rs2290263 7 25847658 intergenic variant G/A snv 0.77 3
rs35004449
ITIH4
3 52818881 3 prime UTR variant G/T snv 0.27 3
rs35716097
SLC34A1
5 177379635 intron variant C/T snv 0.34 3
rs36096257
TFCP2L1
2 121281207 missense variant G/A snv 6.8E-03 2.9E-03 3
rs3795503
LOC107985231 ; KIAA1614
1 180936558 synonymous variant C/T snv 0.31 0.27 3
rs3850625
CACNA1S
1 201047168 missense variant G/A snv 0.12 8.9E-02 3
rs4690095
RGS12
4 3419582 intron variant C/G;T snv 3
rs4715491
FAM83B
6 54899522 intron variant A/G snv 0.17 3
rs549752
LOC107985163 ; NFATC1
18 79398225 intron variant A/G snv 0.40 3
rs6484504
DNAJC24
11 31403276 intron variant T/C snv 0.79 3
rs7012637 8 9315699 intron variant G/A;C snv 3
rs7024579
QSOX2
9 136208567 3 prime UTR variant C/A;T snv 3
rs74183647
LOC107985163 ; NFATC1
18 79396171 5 prime UTR variant G/A;C snv 3
rs7624084
ZBTB38
3 141374443 intron variant T/C snv 0.54 3
rs7766720
LINC02532
6 106725104 non coding transcript exon variant T/C snv 0.16 3