Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 9
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 4
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 4
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 4
rs6569992 6 135131014 intergenic variant G/A;C;T snv 4
rs67250268
H2AC6
6 26135269 intron variant A/-;AA delins 4
rs932316 6 25640972 upstream gene variant T/C;G snv 4
rs169219 6 25957164 intergenic variant C/A;G snv 3
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 3
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 3
rs9483769
LOC101928277
6 134878643 intergenic variant A/G;T snv 3
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 2
rs12718597
IKZF1
7 50360730 intron variant C/A;T snv 2
rs131794
ODF3B
22 50533323 upstream gene variant A/C;G;T snv 2
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 2
rs4466998
MAX ; CHURC1-FNTB ; FNTB
14 65008822 intron variant C/A;G snv 2
rs5749450
FBXO7
22 32490490 non coding transcript exon variant G/A;T snv 2
rs643381 6 139518286 intron variant C/A;G snv 2