Source: GWASDB

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: rs10232025
rs10232025
7 111445562 intron variant T/C snp 9.3E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs1029409
rs1029409
11 2288668 intergenic variant G/A snp 0.49
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs10512730
rs10512730
5 4469660 intron variant G/A snp 0.20; 9.6E-05
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs10970869
rs10970869
9 32255127 intergenic variant G/A snp 0.15
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs112116
rs112116
2 151179196 intron variant T/C snp 0.12
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs1159143
rs1159143
1 216281141 intron variant T/A,G snp 0.67
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs11767630
rs11767630
7 111458717 intron variant A/G snp 9.7E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs11975331
rs11975331
7 111520300 intron variant A/G snp 0.12
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs11979526
rs11979526
7 111600257 intergenic variant A/G snp 7.2E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs12610400
rs12610400
19 55811843 intron variant T/C snp 0.32
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs13290663
rs13290663
9 73204839 intergenic variant C/T snp 0.15
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs1369867
rs1369867
6 82675433 intergenic variant C/T snp 0.68
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs14130
rs14130
1 68119062 intron variant A/G snp 0.34
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs1553400
rs1553400
1 17715540 intergenic variant A/G snp 0.23
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs16913820
rs16913820
11 5361504 intron variant C/T snp 0.11
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs17042212
rs17042212
1 216300403 intron variant A/G snp 0.16
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs1909492
rs1909492
3 65811865 intron variant T/C snp 0.58
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs2076625
rs2076625
11 33606571 intron variant A/C snp 0.37
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs2137962
rs2137962
8 82515679 intron variant A/G snp 0.64
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs2295193
rs2295193
1.000 0.036 6 152131959 intron variant G/A,C snp 0.61; 3.2E-05
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs2350797
rs2350797
2 155426800 intergenic variant G/A snp 9.8E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs2616943
rs2616943
19 55830208 intron variant G/A snp 0.44
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs2631837
rs2631837
2 54811693 intron variant A/G,T snp 0.87
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs2669057
rs2669057
1 216226680 intron variant C/T snp 0.19
CUI: C0005890
Disease: Body Height
Body Height
0.700 0
dbSNP: rs2885856
rs2885856
2 83968860 intergenic variant T/C snp 0.17
CUI: C0005890
Disease: Body Height
Body Height
0.700 0