rs17020055, VAV3

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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
42 1.000 0.040 1 107793911 intron variant A/C snv 0.11 0.800 1.000 1 2012 2016