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: rs61740466
rs61740466 		1 19608406 non coding transcript exon variant G/A snv 0.26 0.20
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs12024554
rs12024554 		1 19599265 intron variant C/T snv 0.20
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs12408663
rs12408663 		1 19641564 intron variant T/C snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12408663
rs12408663 		1 19641564 intron variant T/C snv 0.19
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1320978
rs1320978 		1 19621479 intron variant A/G snv 0.64
CUI: C2242456
Disease: thyroid function
thyroid function 		0.700 1.000 1 2012 2012
dbSNP: rs2745217
rs2745217 		1 19595253 intron variant C/T snv 0.64
CUI: C2242456
Disease: thyroid function
thyroid function 		0.700 1.000 1 2012 2012
dbSNP: rs2792043
rs2792043 		1 19598168 non coding transcript exon variant A/C snv 0.64
CUI: C2242456
Disease: thyroid function
thyroid function 		0.700 1.000 1 2012 2012
dbSNP: rs372271081
rs372271081 		1.000 0.080 1 19647903 intron variant G/A snv 8.4E-02
CUI: C0151526
Disease: Premature Birth
Premature Birth 		Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2018 2018
dbSNP: rs372271081
rs372271081 		1.000 0.080 1 19647903 intron variant G/A snv 8.4E-02
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7546665
rs7546665 		1 19654530 intron variant T/C snv 0.42
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019