rs138206701, RASGRF2

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Eating Disorders
CUI: C0013473
Disease: Eating Disorders
42 5 81110747 intron variant A/G snv 1.7E-02 0.700 1.000 1 2013 2013
Other eating disorders
CUI: C0029587
Disease: Other eating disorders
11 5 81110747 intron variant A/G snv 1.7E-02 0.700 1.000 1 2013 2013