Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10236314
rs10236314
7 20676586 intron variant A/C snv 0.90
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10456943
rs10456943
6 121556819 regulatory region variant A/C snv 0.11
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10799445
rs10799445
1 227724182 upstream gene variant A/C snv 0.27
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
dbSNP: rs10974438
rs10974438
0.925 0.120 9 4291928 intron variant A/C snv 0.29
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs11198898
rs11198898
10 119358980 intron variant A/C snv 0.79
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs11521830
rs11521830
9 75675924 intergenic variant A/C snv 5.6E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs11542436
rs11542436
17 63701329 non coding transcript exon variant A/C snv 0.30
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs11638850
rs11638850
15 56141657 intron variant A/C snv 0.63
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12003361
rs12003361
9 120093136 intergenic variant A/C snv 9.8E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12076549
rs12076549
1 91736142 intron variant A/C snv 0.53
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12309133
rs12309133
12 81843061 intergenic variant A/C snv 0.37
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12347137
rs12347137
9 116360442 intron variant A/C snv 0.16
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12459174
rs12459174
19 57293351 3 prime UTR variant A/C snv 0.23
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12676304
rs12676304
8 128151049 intron variant A/C snv 0.24
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12903859
rs12903859
15 70493294 intergenic variant A/C snv 0.84
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12909519
rs12909519
15 51049670 intron variant A/C snv 0.60
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs13002867
rs13002867
2 171298866 intergenic variant A/C snv 0.23
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1303630
rs1303630
3 25504009 intron variant A/C snv 0.61
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs13093889
rs13093889
3 8958363 intron variant A/C snv 0.17
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs13244629
rs13244629
7 100911633 intergenic variant A/C snv 0.14
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs13393256
rs13393256
2 47059620 intron variant A/C snv 0.72
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1366594
rs1366594
5 89080244 intron variant A/C snv 0.57
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs141604861
rs141604861
13 49822570 intergenic variant A/C snv 5.8E-03
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs141704717
rs141704717
6 130391974 intron variant A/C snv 8.5E-03
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs143668036
rs143668036
1 66129143 intron variant A/C snv 1.3E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019