rs776935407, SGSM3

N. diseases: 6
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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 0.010 1.000 1 2011 2011
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 0.010 1.000 1 2011 2011
melanoma
CUI: C0025202
Disease: melanoma
515 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 0.010 1 2005 2005
Nevi and Melanomas
CUI: C0206769
Disease: Nevi and Melanomas
3 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 0.010 1.000 1 2005 2005
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 0.010 1.000 1 2011 2011
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 0.010 1.000 1 2011 2011