Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 4
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 3
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 3
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 3
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 2
rs9389268
HBS1L
1.000 0.080 6 135098493 intron variant A/G snv 0.24 2
rs11107
FBXO7
1.000 0.040 22 32479203 start lost G/A;C snv 0.45; 8.0E-06 1
rs6729815
BCL11A
1.000 0.080 2 60496537 intron variant T/C snv 0.49 1
rs6776003
RASA2
1.000 0.080 3 141547651 intron variant G/A snv 0.55 1
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 1
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 5
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 3
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
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 5