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: rs10116857
rs10116857
BNC2
9 16595651 intron variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs10756785
rs10756785
BNC2
0.925 0.040 9 16700839 intron variant C/T snv 0.60
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs10756785
rs10756785
BNC2
0.925 0.040 9 16700839 intron variant C/T snv 0.60
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs10756796
rs10756796
BNC2
1.000 0.040 9 16730976 intron variant A/G snv 0.43
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs10810603
rs10810603
BNC2
9 16740857 intron variant G/A snv 0.22
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10810635
rs10810635
BNC2
1.000 0.040 9 16795243 intron variant T/C snv 9.0E-02
CUI: C0025209
Disease: Melanosis
Melanosis 		0.700 1.000 1 2018 2018
dbSNP: rs10962547
rs10962547
BNC2
9 16712249 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs10962599
rs10962599
BNC2
9 16795288 intron variant C/A;T snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs10962612
rs10962612
BNC2
9 16804169 intron variant T/G snv 0.50
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018
dbSNP: rs10962638
rs10962638
BNC2
9 16846113 intron variant G/A;C snv
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs12335424
rs12335424
BNC2
9 16692106 intron variant C/T snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1411431
rs1411431
BNC2
9 16728723 intron variant C/A snv 0.17
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1411432
rs1411432
BNC2
9 16728534 intron variant A/C snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1538101
rs1538101
BNC2
9 16710872 intron variant A/G snv 0.90
CUI: C4280669
Disease: Velopharyngeal dysfunction
Velopharyngeal dysfunction 		0.700 1.000 1 2018 2018
dbSNP: rs17743593
rs17743593
BNC2
9 16809960 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs189669683
rs189669683
BNC2
1.000 0.040 9 16810447 intron variant G/C snv 2.1E-04
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs189669683
rs189669683
BNC2
1.000 0.040 9 16810447 intron variant G/C snv 2.1E-04
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2015 2015
dbSNP: rs2153271
rs2153271
BNC2
0.925 0.160 9 16864523 intron variant C/T snv 0.43
CUI: C0025209
Disease: Melanosis
Melanosis 		0.700 1.000 1 2010 2010
dbSNP: rs3850445
rs3850445
BNC2
9 16703383 intron variant A/G snv 0.60
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs3904778
rs3904778
BNC2
0.882 0.200 9 16681995 intron variant C/G snv 0.62
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2015 2015
dbSNP: rs3904778
rs3904778
BNC2
0.882 0.200 9 16681995 intron variant C/G snv 0.62
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2015 2015
dbSNP: rs4961737
rs4961737
BNC2
9 16721069 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7028900
rs7028900
BNC2
0.925 0.040 9 16690614 intron variant G/C snv 0.61
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2019 2019
dbSNP: rs7028900
rs7028900
BNC2
0.925 0.040 9 16690614 intron variant G/C snv 0.61
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs73646205
rs73646205
BNC2
9 16724057 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019