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rs755322824

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755322824(C;C)
Make rs755322824(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position533790
GeneHRAS, LRRC56
is asnp
is mentioned by
dbSNPrs755322824
ebirs755322824
HLIrs755322824
Exacrs755322824
Varsomers755322824
Maprs755322824
PheGenIrs755322824
hapmaprs755322824
1000 genomesrs755322824
hgdprs755322824
ensemblrs755322824
gopubmedrs755322824
geneviewrs755322824
scholarrs755322824
googlers755322824
pharmgkbrs755322824
gwascentralrs755322824
openSNPrs755322824
23andMers755322824
23andMe allrs755322824
SNP Nexus

SNPshotrs755322824
SNPdbers755322824
MSV3drs755322824
GWAS Ctlgrs755322824
Max Magnitude0
ClinVar
Risk rs755322824(C;C)
Alt rs755322824(C;C)
Reference rs755322824(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HRAS
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.533790G>C
CLNSRC
CLNACC RCV000207497.1,