GOLGA2, golgin A2, 2801

N. diseases: 29; N. variants: 3
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: rs113132247
rs113132247
9 128263829 intron variant G/A snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs4734
rs4734
9 128256360 3 prime UTR variant T/G snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs7871866
rs7871866
9 128265703 intron variant G/C snv 0.17 0.15
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019