rs17064002, None

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.
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 13 42996665 upstream gene variant C/T snv 1.8E-02 0.700 1.000 1 2012 2012
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 13 42996665 upstream gene variant C/T snv 1.8E-02 0.700 1.000 1 2012 2012