Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10913469
rs10913469 		1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C0005910
Disease: Body Weight
Body Weight 		Pathological Conditions, Signs and Symptoms 0.800 1.000 1 2009 2009
dbSNP: rs10913469
rs10913469 		1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.720 0.667 3 2009 2013
dbSNP: rs10913469
rs10913469 		1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2009 2019
dbSNP: rs545608
rs545608 		0.925 0.040 1 177929986 intron variant G/C snv 0.20
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2019
dbSNP: rs591120
rs591120 		1 177933618 missense variant G/A;C snv 4.0E-06; 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2015 2018
dbSNP: rs10913469
rs10913469 		1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2009 2009
dbSNP: rs10913469
rs10913469 		1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2019 2019
dbSNP: rs10913469
rs10913469 		1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2010 2010
dbSNP: rs10913469
rs10913469 		1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2009 2009
dbSNP: rs506589
rs506589 		1 177925152 intron variant T/C snv 0.21
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs545608
rs545608 		0.925 0.040 1 177929986 intron variant G/C snv 0.20
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs545608
rs545608 		0.925 0.040 1 177929986 intron variant G/C snv 0.20
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs545608
rs545608 		0.925 0.040 1 177929986 intron variant G/C snv 0.20
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs591120
rs591120 		1 177933618 missense variant G/A;C snv 4.0E-06; 0.42
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2013 2013
dbSNP: rs591120
rs591120 		1 177933618 missense variant G/A;C snv 4.0E-06; 0.42
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013