Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894226(A;A)
Make rs104894226(A;G)
ReferenceGRCh37 37.1/132
Chromosome11
Position534285
GeneHRAS
is asnp
is mentioned by
dbSNPrs104894226
ClinGenrs104894226
ebirs104894226
HLIrs104894226
Exacrs104894226
Varsomers104894226
Maprs104894226
PheGenIrs104894226
hapmaprs104894226
1000 genomesrs104894226
hgdprs104894226
ensemblrs104894226
gopubmedrs104894226
geneviewrs104894226
scholarrs104894226
googlers104894226
pharmgkbrs104894226
gwascentralrs104894226
openSNPrs104894226
23andMers104894226
23andMe allrs104894226
SNP Nexus

SNPshotrs104894226
SNPdbers104894226
MSV3drs104894226
GWAS Ctlgrs104894226
Max Magnitude0
OMIM190020
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894226(A;A) rs104894226(C;C) rs104894226(T;T)
Alt rs104894226(A;A) rs104894226(C;C) rs104894226(T;T)
Reference Rs104894226(G;G)
Significance Pathogenic
Disease not provided Chronic lymphocytic leukemia Hepatocellular carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Colorectal Neoplasms Multiple myeloma Acute myeloid leukemia Adenocarcinoma of stomach Squamous cell carcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Thymoma Neoplasm of breast Uterine cervical neoplasms Costello syndrome
Variation info
Gene HRAS
CLNDBN not provided Chronic lymphocytic leukemia Hepatocellular carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Colorectal Neoplasms Multiple myeloma Acute myeloid leukemia Adenocarcinoma of stomach Squamous cell carcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Thymoma Neoplasm of breast Uterine cervical neoplasms Costello syndrome
Reversed 1
HGVS NC_000011.9:g.534285C>A; NC_000011.9:g.534285C>G; NC_000011.9:g.534285C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000157914.1, RCV000418565.1, RCV000418712.1, RCV000419846.1, RCV000421468.1, RCV000424767.1, RCV000426169.1, RCV000427265.1, RCV000428389.1, RCV000429433.1, RCV000432148.1, RCV000434580.1, RCV000436822.1, RCV000437080.1, RCV000439230.1, RCV000442670.1, RCV000444507.1, RCV000444587.1, RCV000421384.1, RCV000424186.1, RCV000425652.1, RCV000426316.1, RCV000433957.1, RCV000434248.1, RCV000434457.1, RCV000440965.1, RCV000442365.1, RCV000445345.1, RCV000013438.24, RCV000157913.2, RCV000439514.1,