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: rs10913469
rs10913469
1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 1 2009 2009
dbSNP: rs591120
rs591120
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 1 2013 2013