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rs28933406

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(G;G) 0
Make rs28933406(A;A)
Make rs28933406(A;C)
ReferenceGRCh37 37.1/131
Chromosome11
Position533875
GeneHRAS
is asnp
is mentioned by
dbSNPrs28933406
ebirs28933406
HLIrs28933406
Exacrs28933406
Varsomers28933406
Maprs28933406
PheGenIrs28933406
hapmaprs28933406
1000 genomesrs28933406
hgdprs28933406
ensemblrs28933406
gopubmedrs28933406
geneviewrs28933406
scholarrs28933406
googlers28933406
pharmgkbrs28933406
gwascentralrs28933406
openSNPrs28933406
23andMers28933406
23andMe allrs28933406
SNP Nexus

SNPshotrs28933406
SNPdbers28933406
MSV3drs28933406
GWAS Ctlgrs28933406
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM190020
DescTHYROID CARCINOMA, FOLLICULAR, SOMATIC
Variant0002
Relatedalso


ClinVar
Risk rs28933406(A;A)
Alt rs28933406(A;A)
Reference rs28933406(C;C)
Significance Pathogenic
Disease Thyroid cancer Spermatocytic seminoma
Variation info
Gene HRAS
CLNDBN Thyroid cancer, follicular Spermatocytic seminoma
Reversed 1
HGVS NC_000011.9:g.533875G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013434.6, RCV000022795.6,