rs17601696, 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.
Deglutition Disorders
CUI: C0011168
Disease: Deglutition Disorders
50 10 121360522 intergenic variant C/T snv 6.0E-02 0.700 1.000 1 2015 2015
Swallowing problem
CUI: C0392678
Disease: Swallowing problem
1 10 121360522 intergenic variant C/T snv 6.0E-02 0.010 1.000 1 2015 2015