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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2012 2018
dbSNP: rs10510419
rs10510419
3 12385437 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs11709077
rs11709077
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2015 2015
dbSNP: rs17036328
rs17036328
1.000 0.040 3 12348985 intron variant T/C snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs1899951
rs1899951
0.851 0.160 3 12353341 intron variant C/T snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017