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rs121913233

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913233(A;T)
Make rs121913233(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position533874
GeneHRAS, LRRC56
is asnp
is mentioned by
dbSNPrs121913233
dbSNP (old)rs121913233
ClinGenrs121913233
ebirs121913233
HLIrs121913233
Exacrs121913233
Gnomadrs121913233
Varsomers121913233
Maprs121913233
PheGenIrs121913233
Biobankrs121913233
1000 genomesrs121913233
hgdprs121913233
ensemblrs121913233
gopubmedrs121913233
geneviewrs121913233
scholarrs121913233
googlers121913233
pharmgkbrs121913233
gwascentralrs121913233
openSNPrs121913233
23andMers121913233
23andMe allrs121913233
SNP Nexus

SNPshotrs121913233
SNPdbers121913233
MSV3drs121913233
GWAS Ctlgrs121913233
Max Magnitude0
ClinVar
Risk rs121913233(C;C) rs121913233(G;G) rs121913233(T;T)
Alt rs121913233(C;C) rs121913233(G;G) rs121913233(T;T)
Reference Rs121913233(A;A)
Significance Pathogenic
Disease Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Colorectal Neoplasms Malignant neoplasm of body of uterus Malignant melanoma of skin Pancreatic adenocarcinoma Acute myeloid leukemia Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Chronic lymphocytic leukemia Adenocarcinoma of lung Squamous cell carcinoma of lung Multiple myeloma Adenocarcinoma of prostate Neoplasm of breast Neoplasm of the thyroid gland Squamous cell carcinoma of the skin Epidermal nevus syndrome not specified Neoplasm
Variation info
Gene HRAS
CLNDBN Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Colorectal Neoplasms Malignant neoplasm of body of uterus Malignant melanoma of skin Pancreatic adenocarcinoma Acute myeloid leukemia Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Chronic lymphocytic leukemia Adenocarcinoma of lung Squamous cell carcinoma of lung Multiple myeloma Adenocarcinoma of prostate Neoplasm of breast Neoplasm of the thyroid gland Squamous cell carcinoma of the skin Epidermal nevus syndrome not specified Neoplasm
Reversed 1
HGVS NC_000011.9:g.533874T>A; NC_000011.9:g.533874T>C; NC_000011.9:g.533874T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000420395.1, RCV000420623.1, RCV000421690.1, RCV000421974.1, RCV000425694.1, RCV000426826.1, RCV000428206.1, RCV000428443.1, RCV000430634.1, RCV000433098.1, RCV000436845.1, RCV000437079.1, RCV000438263.1, RCV000438465.1, RCV000439626.1, RCV000445166.1, RCV000445204.1, RCV000148033.4, RCV000157918.1, RCV000418550.1, RCV000437086.1, RCV000417619.1, RCV000419094.1, RCV000420448.1, RCV000424105.1, RCV000425877.1, RCV000428681.1, RCV000428741.1, RCV000430030.1, RCV000430658.1, RCV000435275.1, RCV000435489.1, RCV000435915.1, RCV000440764.1, RCV000441832.1,