Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6219
rs6219
IGF1 ; HELLPAR ; LINC02456
1.000 0.080 12 102396414 3 prime UTR variant C/T snv 8.9E-02
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2018 2018
dbSNP: rs6219
rs6219
IGF1 ; HELLPAR ; LINC02456
1.000 0.080 12 102396414 3 prime UTR variant C/T snv 8.9E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2018 2018