Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs1035543
PKD1L3
16 71949873 missense variant G/C snv 0.39 0.33 2
rs11030119
BDNF
11 27706555 intron variant G/A;T snv 2
rs11072518 15 74942269 upstream gene variant T/A;C snv 2
rs12037987
WNT2B
1 112500200 intron variant T/C snv 8.6E-02 2
rs10123021 9 100689786 regulatory region variant G/A;T snv 1
rs10414398
CEACAM20
19 44517149 missense variant G/A snv 0.14 0.15 1
rs10890917 11 108988857 intergenic variant C/A;G snv 3.5E-02 1
rs11044400 12 19033113 intergenic variant C/T snv 0.13 1
rs11240065
LINC00624
1 147468451 intron variant T/C snv 1
rs11548491
INPPL1
11 72237492 missense variant C/G;T snv 9.6E-02 1
rs11681884 2 113090051 downstream gene variant C/T snv 0.21 1
rs12291066
MICAL2
11 12213613 intron variant G/A snv 3.6E-02 1
rs12417971 11 69202341 intergenic variant C/T snv 6.4E-02 1
rs12442374 15 56012299 intergenic variant C/G;T snv 1
rs12646447 4 110778170 intergenic variant T/C snv 0.15 1
rs13168506
TGFBI
5 136060763 intron variant A/G snv 0.57 1
rs13407662
ASB3
2 53555422 intron variant C/T snv 4.4E-02 1
rs145067756
UBE2Z
17 48923631 intron variant -/AAACAATGTCACAG;AAAGAATGTCACAG;AAAGAATGTCGCAG;AATGTCACAG;AGAGAATGTCACAG delins 0.40 1
rs148158062
LINC00624
1 147468451 intron variant -/GTTCCTTC delins 1
rs1564060 14 84159449 intergenic variant A/G snv 0.68 1
rs1568362252
NOTCH3
19 15192490 missense variant C/T snv 1
rs161802
PARK7
1 7982766 intron variant G/T snv 0.25 1
rs16851055
SPSB4
3 141080371 non coding transcript exon variant G/A snv 0.26 1
rs17329620 12 87757000 upstream gene variant A/C;G snv 0.11 1