Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6672992
DNAJC6
1 65382351 intron variant A/C snv 0.12 1
rs72675531
LOC105378741
1 56111740 intergenic variant A/C snv 0.26 1
rs75859969 16 50126826 intron variant A/C snv 0.17 1
rs76721774
CUX2
12 111268872 intron variant A/C snv 1.1E-02 1
rs77696237
CDH12
5 22076380 intron variant A/C snv 1.9E-02 1
rs78784853
TXNDC11
16 11723610 intron variant A/C snv 6.4E-02 1
rs8085287
RBBP8
18 22884208 intron variant A/C snv 0.68 1
rs874844
KIRREL1
1 158097257 3 prime UTR variant A/C snv 0.42 1
rs9858874
LSAMP
3 116782013 intron variant A/C snv 7.8E-03 1
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs1512282
LOC105377462
4 144510345 intron variant A/C;G snv 0.33 5
rs8017228
STXBP6
14 24980020 intron variant A/C;G snv 2
rs112389236
LAMA3
18 23903604 intron variant A/C;G snv 1
rs2865805
AUTS2
7 69853209 intron variant A/C;G snv 1
rs311629
S1PR4
19 3180805 upstream gene variant A/C;G snv 1
rs34089598
KLF3
4 38675606 intron variant A/C;G snv 1
rs3820677
KIRREL1
1 158098554 3 prime UTR variant A/C;G snv 1
rs6588216
SGIP1
1 66680164 intron variant A/C;G snv 1
rs67584485
THADA
2 43535056 intron variant A/C;G snv 1
rs6831368
TBC1D14
4 6968192 intron variant A/C;G snv 1
rs9869574
BBX
3 107662804 5 prime UTR variant A/C;G snv 1
rs11039436 11 47866484 intergenic variant A/C;G;T snv 2
rs12034864 1 159215190 regulatory region variant A/C;G;T snv 2
rs4807462
NFIC
19 3408667 intron variant A/C;G;T snv 2
rs10848737
TULP3
12 2911478 intron variant A/C;G;T snv 1