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rs11554290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
(T;T) 0
Make rs11554290(A;G)
Make rs11554290(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position114713908
GeneNRAS
is asnp
is mentioned by
dbSNPrs11554290
ebirs11554290
HLIrs11554290
Exacrs11554290
Varsomers11554290
Maprs11554290
PheGenIrs11554290
hapmaprs11554290
1000 genomesrs11554290
hgdprs11554290
ensemblrs11554290
gopubmedrs11554290
geneviewrs11554290
scholarrs11554290
googlers11554290
pharmgkbrs11554290
gwascentralrs11554290
openSNPrs11554290
23andMers11554290
23andMe allrs11554290
SNP Nexus

SNPshotrs11554290
SNPdbers11554290
MSV3drs11554290
GWAS Ctlgrs11554290
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM164790
DescTHYROID CARCINOMA, FOLLICULAR
Variant0002
Relatedalso


ClinVar
Risk rs11554290(C,G,T;C,G,T)
Alt rs11554290(C,G,T;C,G,T)
Reference rs11554290(A;A)
Significance Pathogenic
Disease Thyroid cancer Epidermal nevus Non-small cell lung cancer Giant pigmented hairy nevus Neurocutaneous melanosis Epidermal nevus syndrome
Variation info
Gene NRAS
CLNDBN Thyroid cancer, follicular Epidermal nevus Non-small cell lung cancer Giant pigmented hairy nevus Neurocutaneous melanosis Epidermal nevus syndrome
Reversed 1
HGVS NC_000001.10:g.115256529T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014914.8, RCV000032847.8, RCV000037574.2, RCV000114744.7, RCV000114745.7, RCV000148032.4,