rs362272, HTT

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.
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 1.000 0.120 4 3233253 missense variant G/A;T snv 0.29 0.700 1.000 1 2012 2012
Sulfate measurement
CUI: C0474702
Disease: Sulfate measurement
3 1.000 0.120 4 3233253 missense variant G/A;T snv 0.29 0.700 1.000 1 2016 2016