Source: GWASDB

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: rs7322916
rs7322916
13 25433839 intron variant G/A;C snv
CUI: C0013473
Disease: Eating Disorders
Eating Disorders
0.800 1.000 1 2013 2013