Source: ALL

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: rs1585775
rs1585775
3 102280281 intron variant T/C snv 8.6E-02
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs9838540
rs9838540
0.925 0.040 3 102267159 intron variant A/C snv 0.49
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs9838540
rs9838540
0.925 0.040 3 102267159 intron variant A/C snv 0.49
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 1 2018 2018
dbSNP: rs985375
rs985375
3 102348402 intron variant G/A snv 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs17822656
rs17822656
3 102470325 intron variant T/C snv 9.5E-02
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
0.010 1.000 1 2018 2018