rs916171, HTT

N. diseases: 1
Source: GWASDB ×
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
41 1.000 0.120 4 3215088 intron variant C/G snv 0.42 0.47 0.700 1.000 1 2012 2012