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: rs12534093
rs12534093 		7 23463355 intron variant T/A snv 0.18
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2019
dbSNP: rs11765649
rs11765649 		7 23439394 intron variant T/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2016 2016
dbSNP: rs118003225
rs118003225 		7 23469676 intron variant C/A;G snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs12534093
rs12534093 		7 23463355 intron variant T/A snv 0.18
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs12534093
rs12534093 		7 23463355 intron variant T/A snv 0.18
CUI: C0455806
Disease: Infant length
Infant length 		0.700 1.000 1 2015 2015
dbSNP: rs3087888
rs3087888 		7 23311461 3 prime UTR variant C/G snv 4.7E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6957923
rs6957923 		7 23443066 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs6957923
rs6957923 		7 23443066 intron variant G/A;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013