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rs727503093

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503093(A;A)
Make rs727503093(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position533881
GeneHRAS, LRRC56
is asnp
is mentioned by
dbSNPrs727503093
ebirs727503093
HLIrs727503093
Exacrs727503093
Varsomers727503093
Maprs727503093
PheGenIrs727503093
hapmaprs727503093
1000 genomesrs727503093
hgdprs727503093
ensemblrs727503093
gopubmedrs727503093
geneviewrs727503093
scholarrs727503093
googlers727503093
pharmgkbrs727503093
gwascentralrs727503093
openSNPrs727503093
23andMers727503093
23andMe allrs727503093
SNP Nexus

SNPshotrs727503093
SNPdbers727503093
MSV3drs727503093
GWAS Ctlgrs727503093
Max Magnitude0
ClinVar
Risk rs727503093(A;A)
Alt rs727503093(A;A)
Reference rs727503093(G;G)
Significance Pathogenic
Disease Non-small cell lung cancer Costello syndrome Rasopathy
Variation info
Gene HRAS
CLNDBN Non-small cell lung cancer Costello syndrome Rasopathy
Reversed 1
HGVS NC_000011.9:g.533881C>T
CLNSRC
CLNACC RCV000150834.1, RCV000150835.1, RCV000157916.1,