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rs730880464

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880464(C;C)
Make rs730880464(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position533535
GeneHRAS, LRRC56
is asnp
is mentioned by
dbSNPrs730880464
ebirs730880464
HLIrs730880464
Exacrs730880464
Varsomers730880464
Maprs730880464
PheGenIrs730880464
hapmaprs730880464
1000 genomesrs730880464
hgdprs730880464
ensemblrs730880464
gopubmedrs730880464
geneviewrs730880464
scholarrs730880464
googlers730880464
pharmgkbrs730880464
gwascentralrs730880464
openSNPrs730880464
23andMers730880464
23andMe allrs730880464
SNP Nexus

SNPshotrs730880464
SNPdbers730880464
MSV3drs730880464
GWAS Ctlgrs730880464
Max Magnitude0
ClinVar
Risk rs730880464(C;C)
Alt rs730880464(C;C)
Reference rs730880464(G;G)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene HRAS
CLNDBN Rasopathy
Reversed 1
HGVS NC_000011.9:g.533535C>G
CLNSRC
CLNACC RCV000157923.1,