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rs267606920

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606920(A;A)
Make rs267606920(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position114713911
GeneNRAS
is asnp
is mentioned by
dbSNPrs267606920
ebirs267606920
HLIrs267606920
Exacrs267606920
Varsomers267606920
Maprs267606920
PheGenIrs267606920
hapmaprs267606920
1000 genomesrs267606920
hgdprs267606920
ensemblrs267606920
gopubmedrs267606920
geneviewrs267606920
scholarrs267606920
googlers267606920
pharmgkbrs267606920
gwascentralrs267606920
openSNPrs267606920
23andMers267606920
23andMe allrs267606920
SNP Nexus

SNPshotrs267606920
SNPdbers267606920
MSV3drs267606920
GWAS Ctlgrs267606920
Max Magnitude0
ClinVar
Risk rs267606920(A;A)
Alt rs267606920(A;A)
Reference rs267606920(G;G)
Significance Pathogenic
Disease Noonan syndrome 6 not provided Noonan syndrome 1
Variation info
Gene NRAS
CLNDBN Noonan syndrome 6 not provided Noonan syndrome 1
Reversed 1
HGVS NC_000001.10:g.115256532C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014917.25, RCV000158982.2, RCV000208552.1,