rs10004195, TLR10

N. diseases: 8
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.
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.700 1.000 1 2013 2013
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2015 2015
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2015 2015
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2019 2019
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2011 2011
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2015 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2015 2015
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2015 2015