Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1408272
SLC17A3
6 25842723 intron variant T/G snv 4.0E-02 3
rs632057 6 139512875 intron variant T/G snv 0.57 3
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 3
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
rs4820091
UBE2L3
22 21585900 intron variant T/G snv 0.30 1
rs6904897
HBS1L
6 135061842 intron variant T/G snv 0.34 1
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs932316 6 25640972 upstream gene variant T/C;G snv 4
rs6899876
USP49
6 41829232 intron variant T/C;G snv 0.23 3
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 1
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs3115663
PRRC2A ; MIR6832
0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs17064262 6 135144336 intergenic variant T/C snv 0.18 4
rs8141597
MPST
22 37028807 non coding transcript exon variant T/C snv 0.31 4
rs13027161
MIR4432HG
2 60380593 intron variant T/C snv 0.29 3
rs2235324
TMPRSS6
22 37089684 missense variant T/C snv 0.38 0.40 3
rs2236496
RCL1
9 4844265 intron variant T/C snv 0.19 3
rs2540917
MIR4432HG
2 60381624 intron variant T/C snv 0.29 3
rs5994574 22 32470947 upstream gene variant T/C snv 0.46 3
rs12718598
IKZF1
7 50360747 intron variant T/C snv 0.50 2
rs9374080
CCDC162P
6 109295217 intron variant T/C snv 0.40 2
rs9389269
LOC105378010
6 135106021 upstream gene variant T/C snv 0.20 2
rs9494142
LOC105378010
6 135110502 TF binding site variant T/C snv 0.21 2
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 1