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rs730880461

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880461(A;A)
Make rs730880461(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position533853
GeneHRAS, LRRC56
is asnp
is mentioned by
dbSNPrs730880461
ebirs730880461
HLIrs730880461
Exacrs730880461
Varsomers730880461
Maprs730880461
PheGenIrs730880461
hapmaprs730880461
1000 genomesrs730880461
hgdprs730880461
ensemblrs730880461
gopubmedrs730880461
geneviewrs730880461
scholarrs730880461
googlers730880461
pharmgkbrs730880461
gwascentralrs730880461
openSNPrs730880461
23andMers730880461
23andMe allrs730880461
SNP Nexus

SNPshotrs730880461
SNPdbers730880461
MSV3drs730880461
GWAS Ctlgrs730880461
Max Magnitude0
ClinVar
Risk rs730880461(A;A)
Alt rs730880461(A;A)
Reference rs730880461(G;G)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene HRAS
CLNDBN Rasopathy
Reversed 1
HGVS NC_000011.9:g.533853C>T
CLNSRC
CLNACC RCV000157919.1,