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rs1057519855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1057519855(AG;GT)
Make rs1057519855(GT;GT)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position533873
GeneHRAS, LRRC56
is asnp
is mentioned by
dbSNPrs1057519855
dbSNP (old)rs1057519855
ClinGenrs1057519855
ebirs1057519855
HLIrs1057519855
Exacrs1057519855
Gnomadrs1057519855
Varsomers1057519855
LitVarrs1057519855
Maprs1057519855
PheGenIrs1057519855
Biobankrs1057519855
1000 genomesrs1057519855
hgdprs1057519855
ensemblrs1057519855
gopubmedrs1057519855
geneviewrs1057519855
scholarrs1057519855
googlers1057519855
pharmgkbrs1057519855
gwascentralrs1057519855
openSNPrs1057519855
23andMers1057519855
23andMe allrs1057519855
SNPshotrs1057519855
SNPdbers1057519855
MSV3drs1057519855
GWAS Ctlgrs1057519855
Max Magnitude0
ClinVar
Risk rs1057519855(GA;GA) rs1057519855(GT;GT)
Alt rs1057519855(GA;GA) rs1057519855(GT;GT)
Reference Rs1057519855(AG;AG)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene HRAS
CLNDBN Neoplasm
Reversed 1
HGVS NC_000011.9:g.533873_533874delCTinsAC; NC_000011.9:g.533873_533874delCTinsTC
CLNSRC
CLNACC RCV000435225.1, RCV000418005.1,