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: rs11748619
rs11748619 		5 180300399 downstream gene variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2303009
rs2303009 		5 180318607 intron variant A/G snv 0.11
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6879260
rs6879260 		5 180304014 intron variant T/C snv 0.56
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs6879260
rs6879260 		5 180304014 intron variant T/C snv 0.56
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs193143625
rs193143625 		1.000 0.040 5 180316819 missense variant C/T snv 5.3E-04 4.6E-04
CUI: C0403823
Disease: Asthenozoospermia
Asthenozoospermia 		Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2303007
rs2303007 		1.000 0.080 5 180313827 missense variant T/C snv 0.22 0.18
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2004 2004