rs2269499, HTT

N. diseases: 1
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.
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 1.000 0.120 4 3237975 intron variant C/T snv 0.24 0.700 1.000 1 2012 2012