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: rs10157941
rs10157941
1 53083314 intron variant C/G snv 0.25
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10218741
rs10218741
1 221106893 regulatory region variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10305677
rs10305677
1 150846616 intron variant T/A snv 1.8E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1044145
rs1044145
1 207044014 3 prime UTR variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1044299
rs1044299
1 176842737 3 prime UTR variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10482795
rs10482795
1 218432267 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10737515
rs10737515
1 165630223 upstream gene variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10779364
rs10779364
1 219614071 upstream gene variant G/C snv 0.56
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10793765
rs10793765
1 204580247 intergenic variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10797816
rs10797816
1 183029351 intron variant A/T snv 0.54
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10798580
rs10798580
1 177895419 intron variant G/A snv 0.36
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: rs10857961
rs10857961
1 112539531 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10863936
rs10863936
DTL
1 212064456 intron variant G/A snv 0.59
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
dbSNP: rs10864136
rs10864136
1 214865244 intergenic variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10874746
rs10874746
1 92858414 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
dbSNP: rs10888713
rs10888713
1 50997752 intergenic variant A/T snv 0.11
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10908505
rs10908505
1 156498451 intron variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10911212
rs10911212
1 183055334 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10914505
rs10914505
1 31927977 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10916606
rs10916606
1 224382723 downstream gene variant C/T snv 0.77
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10917123
rs10917123
1 22029485 intron variant G/A snv 0.21
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10922478
rs10922478
1 88678370 intron variant A/G snv 0.61
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1106287
rs1106287
1 112699500 non coding transcript exon variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs11118346
rs11118346
1 219570377 intergenic variant C/T snv 0.38
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010