rs28933406

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(G;G)	0

Reference

GRCh37 37.1/131

Chromosome

11

Position

533875

Gene	HRAS, LRRC56

0

NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

OMIM	190020
Desc	THYROID CARCINOMA, FOLLICULAR, SOMATIC
Variant	0002
Related	also

ClinVar
Risk	rs28933406(A;A) Rs28933406(G;G)
Alt	rs28933406(A;A) Rs28933406(G;G)
Reference	Rs28933406(C;C)
Significance	Pathogenic
Disease	Chronic lymphocytic leukemia Malignant melanoma of skin Pancreatic adenocarcinoma Neoplasm of the thyroid gland Hepatocellular carcinoma Adenocarcinoma of stomach Squamous cell carcinoma of lung Transitional cell carcinoma of the bladder Acute myeloid leukemia Colorectal Neoplasms Malignant neoplasm of body of uterus Multiple myeloma Adenocarcinoma of lung Thyroid cancer Spermatocytic seminoma Neoplasm of breast
Variation	info
Gene	HRAS
CLNDBN	Chronic lymphocytic leukemia Malignant melanoma of skin Pancreatic adenocarcinoma Neoplasm of the thyroid gland Hepatocellular carcinoma Adenocarcinoma of stomach Squamous cell carcinoma of lung Transitional cell carcinoma of the bladder Acute myeloid leukemia Colorectal Neoplasms Malignant neoplasm of body of uterus Multiple myeloma Adenocarcinoma of lung Thyroid cancer, follicular Spermatocytic seminoma Neoplasm of breast
Reversed	1
HGVS	NC_000011.9:g.533875G>C; NC_000011.9:g.533875G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000420757.1, RCV000422470.1, RCV000423098.1, RCV000424391.1, RCV000427302.1, RCV000431015.1, RCV000432499.1, RCV000432733.1, RCV000435578.1, RCV000437532.1, RCV000442518.1, RCV000444550.1, RCV000444619.1, RCV000013434.8, RCV000022795.8, RCV000439343.1,