Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116009877 6 25715429 regulatory region variant G/A;T snv 4
rs13191659
LINC00240
6 27033276 intron variant C/G;T snv 4
rs183252871
EPHB1
3 134964503 intron variant T/C;G snv 2
rs7637997
RAB6B
3 133864120 intron variant G/A;C;T snv 2
rs78455250 1 189052039 intergenic variant G/A;C snv 2
rs78545713
H4C7
6 26248612 upstream gene variant A/G;T snv 2
rs9872999
TF ; INHCAP
3 133738670 intron variant C/G;T snv 2
rs187281066
CPNE4
3 132157410 intron variant A/G snv 1.4E-05 2
rs183511413
TMEM108
3 133330418 intron variant A/G snv 2.3E-04 2
rs192622883
TMEM108
3 133150563 intron variant A/G snv 2.5E-04 2
rs187472012
EPHB1
3 134820915 intron variant A/G snv 2.7E-04 2
rs145285408
LOC105375153
7 11345523 intron variant G/C snv 2.4E-03 2
rs183360145
CARMIL1 ; CMAHP
6 25296893 intron variant T/C snv 2.6E-03 2
rs74138220
LOC105371657
1 189188129 intergenic variant G/A snv 3.8E-03 2
rs144403535 2 62178025 regulatory region variant A/G snv 3.8E-03 2
rs142692454
LOC105378648 ; LOC107984941
1 36686538 intergenic variant A/G snv 4.1E-03 2
rs16839481
NPHP3-ACAD11 ; ACAD11 ; UBA5
3 132660153 5 prime UTR variant G/A snv 1.1E-02 2
rs112409831
DNAJC13
3 132417596 5 prime UTR variant C/T snv 2.3E-02 2
rs9813476
LMLN
3 197992314 intron variant C/T snv 3.7E-02 2
rs80215559
SLC17A2
6 25917997 intron variant T/C snv 3.7E-02 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs61740410
PRSS16
6 27256809 downstream gene variant G/A snv 4.2E-02 2
rs71559014 6 27154665 regulatory region variant A/G snv 4.2E-02 4
rs61784830 1 45763401 intergenic variant G/A snv 8.9E-02 2
rs56071727
CCDC17
1 45625172 upstream gene variant G/T snv 9.0E-02 2