Disease: Bone Mineral Density Test
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 4
rs6959212 7 38088724 intergenic variant T/C;G snv 3
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 2
rs10876432
SP7
12 53338107 intron variant G/A snv 2
rs12407028
GNG12-AS1 ; WLS
1 68182033 intron variant T/A;C snv 0.35 2
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 2
rs1430740
GNG12-AS1 ; WLS
1 68191827 intron variant T/C snv 0.58 2
rs2016266
SP7
1.000 0.080 12 53334171 intron variant G/A;C snv 2
rs2062377
COLEC10
8 118995181 upstream gene variant T/A snv 0.67 2
rs227584
HROB
17 44148179 missense variant A/C snv 0.40 0.48 2
rs2504063
LOC107986529 ; ESR1
6 151769572 intron variant A/G snv 0.50 2
rs4233949
LOC102724072
2 54432570 regulatory region variant C/A;G snv 2
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 2
rs4424296
COLEC10
8 119001037 intron variant C/T snv 0.61 2
rs4727338
SEM1 ; LOC105375411
7 96491363 intron variant G/C;T snv 2
rs4869742
CCDC170
6 151586613 intron variant C/A;G;T snv 2
rs6426749 1.000 0.080 1 22384980 intergenic variant G/C snv 0.19 2
rs6532023 1.000 0.080 4 87852697 regulatory region variant T/G snv 0.66 2
rs6909279
CCDC170
6 151574321 intron variant G/C;T snv 2
rs7751941 6 151625523 downstream gene variant G/A;T snv 2
rs7839059
COLEC10
8 118964303 intergenic variant C/A snv 0.40 2
rs7932354
ARHGAP1 ; ZNF408
11 46700671 upstream gene variant T/C snv 0.53 2
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 2
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39 2