Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894171
rs104894171
MINPP1
1.000 10 87508507 missense variant A/G snv
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
THYROID CANCER, NONMEDULLARY, 2 		0.800 1.000 1 2001 2001
dbSNP: rs114817817
rs114817817
SRGAP1 ; LOC105369798
1.000 12 64108967 missense variant C/T snv 1.1E-03 9.9E-04
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
THYROID CANCER, NONMEDULLARY, 2 		0.800 1.000 1 2013 2013
dbSNP: rs28933406
rs28933406
HRAS ; LRRC56
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
THYROID CANCER, NONMEDULLARY, 2 		0.800 1.000 1 2003 2003
dbSNP: rs781626187
rs781626187
SRGAP1 ; LOC105369801
1.000 12 64016970 missense variant A/C;T snv 2.9E-05; 4.1E-06
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
THYROID CANCER, NONMEDULLARY, 2 		0.800 1.000 1 2013 2013
dbSNP: rs11554290
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
THYROID CANCER, NONMEDULLARY, 2 		0.800 0
dbSNP: rs119486096
rs119486096
MINPP1 ; LOC112268064
1.000 10 87505037 missense variant C/T snv
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
THYROID CANCER, NONMEDULLARY, 2 		0.800 0
dbSNP: rs797044990
rs797044990
SRGAP1
1.000 12 64062938 missense variant G/A snv
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
THYROID CANCER, NONMEDULLARY, 2 		0.800 0
dbSNP: rs61754221
rs61754221
SRGAP1 ; LOC105369798
1.000 12 64127944 missense variant A/C;G snv 7.3E-03
CUI: C4225426
Disease: THYROID CANCER, NONMEDULLARY, 2
THYROID CANCER, NONMEDULLARY, 2 		0.700 0