Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12044963
KCND3
1.000 0.080 1 111849738 intron variant G/T snv 0.10 2
rs10489759 1 189620209 regulatory region variant C/T snv 0.17 1
rs10495471
GREM2
1 240542807 intron variant A/G snv 0.11 1
rs2501276
CDC42-AS1 ; CDC42
1 22047131 intron variant C/T snv 8.1E-02 1
rs316274
RASAL2
1 178173073 intron variant G/A snv 0.26 1
rs4839431
CYMP ; CYMP-AS1
1 110491187 non coding transcript exon variant T/A;C snv 1
rs6679454
DAB1
1 57901564 intron variant A/G snv 0.29 1
rs908327
LOC105373211 ; LOC101927851
1 234956853 upstream gene variant A/C;G snv 1.5E-02 1
rs11889798
C2orf83 ; LOC729968
1.000 0.120 2 227616703 intron variant C/T snv 0.13 2
rs10195263 2 150869278 intergenic variant G/A;C snv 1
rs10432496 2 149290764 regulatory region variant C/A;T snv 1
rs13006863
SLC4A5
2 74236439 intron variant C/T snv 0.26 1
rs13414205
CAMKMT
2 44435336 intron variant C/T snv 3.3E-02 1
rs17007761 2 122468047 intron variant C/A snv 6.0E-02 1
rs2272205
COL4A4
2 227051208 intron variant T/C snv 9.1E-02 7.7E-02 1
rs4078978
WDR92
2 68132765 intron variant C/T snv 6.7E-02 1
rs542631
LTBP1
2 33076880 intron variant T/G snv 0.88 1
rs6728021
LOC105374453 ; LINC00486
2 32896437 intron variant A/G snv 7.9E-02 1
rs10513432 3 152817576 regulatory region variant T/C snv 0.12 1
rs13067593
LPP
3 188866891 intron variant A/G snv 0.12 1
rs13088281
RFT1
3 53113560 intron variant C/A snv 7.6E-02 1
rs1516489
LOC105374276
3 191804063 intergenic variant A/C snv 8.8E-02 1
rs17331151 3 52810518 downstream gene variant C/T snv 7.5E-02 1
rs3796352
STIMATE ; STIMATE-MUSTN1
3 52879263 intron variant C/T snv 6.6E-02 1
rs3804795
IL5RA
3 3088961 intron variant T/C snv 7.5E-02 1