Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10930046
rs10930046
0.882 0.200 2 162281473 missense variant T/C snv 9.7E-02 0.16
CUI: C0178468
Disease: Autoimmune thyroid disease
Autoimmune thyroid disease
Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6432714
rs6432714
0.882 0.160 2 162280842 intron variant A/T snv 0.16
CUI: C0178468
Disease: Autoimmune thyroid disease
Autoimmune thyroid disease
Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2013 2013