Source: CLINVAR

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: rs28933406
rs28933406
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 0 2003 2003
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
Transitional cell carcinoma of bladder
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3
0.700 0
dbSNP: rs28933406
rs28933406
0.667 0.480 11 533875 missense variant G/C;T snv
CUI: C0334517
Disease: Spermatocytic seminoma
Spermatocytic seminoma
0.700 0