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: rs10007975
rs10007975
4 99527667 intron variant C/T snv 0.27
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1000972
rs1000972
20 6641070 regulatory region variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10010325
rs10010325
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
dbSNP: rs10013696
rs10013696
4 6977000 intron variant A/G snv 0.45
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10015974
rs10015974
4 183275101 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10019221
rs10019221
4 21783741 intron variant G/C;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10026360
rs10026360
4 103453439 intron variant T/C snv 0.36
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10031777
rs10031777
4 48496273 downstream gene variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10037743
rs10037743
5 33163672 intron variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10046853
rs10046853
9 14456933 intron variant C/G snv 0.39
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1005502
rs1005502
8 116155618 intron variant C/T snv 0.51
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10058074
rs10058074
5 132350453 intron variant G/A snv 0.31
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2013 2013
dbSNP: rs10059884
rs10059884
5 32832368 regulatory region variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10060053
rs10060053
5 177693696 intron variant T/C snv 0.57
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10061757
rs10061757
5 56790978 intergenic variant G/C snv 0.50
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1006224
rs1006224
1 184572468 intron variant G/A snv 0.40
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1006660
rs1006660
15 89340289 downstream gene variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10073495
rs10073495
5 32160607 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10082444
rs10082444
10 11865983 intron variant T/C snv 0.21
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10088006
rs10088006
8 121652881 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10090382
rs10090382
8 71199443 intron variant T/C snv 0.40 0.35
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10091130
rs10091130
8 130361641 non coding transcript exon variant C/G;T snv 0.77
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1009404
rs1009404
6 113405402 intergenic variant T/C snv 0.71
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10100085
rs10100085
8 40198735 regulatory region variant C/A;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10109417
rs10109417
8 26530784 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019