Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 5
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 5
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs2236496
RCL1
9 4844265 intron variant T/C snv 0.19 5
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs3809627
TBX6 ; YPEL3
16 30091839 5 prime UTR variant C/A snv 0.41 5
rs4449583
TERT
5 1284020 intron variant C/T snv 0.25 5
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 5
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5