Have questions? Visit https://www.reddit.com/r/SNPedia

rs369106578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369106578(A;A)
Make rs369106578(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position533536
GeneHRAS, LRRC56
is asnp
is mentioned by
dbSNPrs369106578
dbSNP (old)rs369106578
ClinGenrs369106578
ebirs369106578
HLIrs369106578
Exacrs369106578
Gnomadrs369106578
Varsomers369106578
Maprs369106578
PheGenIrs369106578
Biobankrs369106578
1000 genomesrs369106578
hgdprs369106578
ensemblrs369106578
gopubmedrs369106578
geneviewrs369106578
scholarrs369106578
googlers369106578
pharmgkbrs369106578
gwascentralrs369106578
openSNPrs369106578
23andMers369106578
23andMe allrs369106578
SNP Nexus

SNPshotrs369106578
SNPdbers369106578
MSV3drs369106578
GWAS Ctlgrs369106578
Max Magnitude0
ClinVar
Risk rs369106578(A;A)
Alt rs369106578(A;A)
Reference Rs369106578(G;G)
Significance Probable-Pathogenic
Disease not provided Costello syndrome
Variation info
Gene HRAS
CLNDBN not provided Costello syndrome
Reversed 0
HGVS NC_000011.9:g.533536G>A
CLNSRC
CLNACC RCV000157922.2, RCV000471505.1,