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rs730880460

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880460(A;A)
Make rs730880460(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position533877
GeneHRAS, LRRC56
is asnp
is mentioned by
dbSNPrs730880460
ebirs730880460
HLIrs730880460
Exacrs730880460
Varsomers730880460
Maprs730880460
PheGenIrs730880460
hapmaprs730880460
1000 genomesrs730880460
hgdprs730880460
ensemblrs730880460
gopubmedrs730880460
geneviewrs730880460
scholarrs730880460
googlers730880460
pharmgkbrs730880460
gwascentralrs730880460
openSNPrs730880460
23andMers730880460
23andMe allrs730880460
SNP Nexus

SNPshotrs730880460
SNPdbers730880460
MSV3drs730880460
GWAS Ctlgrs730880460
Max Magnitude0
ClinVar
Risk rs730880460(A;A)
Alt rs730880460(A;A)
Reference rs730880460(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene HRAS
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.533877C>T
CLNSRC
CLNACC RCV000157917.1,