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: rs13279522
rs13279522 		1.000 0.040 8 66062017 intron variant T/C snv 0.33
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.710 1.000 1 2012 2012
dbSNP: rs11995702
rs11995702 		8 66014188 intergenic variant A/G snv 0.48
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs17398234
rs17398234 		8 66022667 intron variant T/C;G snv
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7832776
rs7832776 		8 66040206 intron variant A/G snv 0.52
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019