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rs113954997

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs113954997(A;T)
Make rs113954997(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position14294844
GeneRRAS2
is asnp
is mentioned by
dbSNPrs113954997
ebirs113954997
HLIrs113954997
Exacrs113954997
Varsomers113954997
Maprs113954997
PheGenIrs113954997
hapmaprs113954997
1000 genomesrs113954997
hgdprs113954997
ensemblrs113954997
gopubmedrs113954997
geneviewrs113954997
scholarrs113954997
googlers113954997
pharmgkbrs113954997
gwascentralrs113954997
openSNPrs113954997
23andMers113954997
23andMe allrs113954997
SNP Nexus

SNPshotrs113954997
SNPdbers113954997
MSV3drs113954997
GWAS Ctlgrs113954997
Max Magnitude0
OMIM600098
Desc
Variant0001
Relatedalso
ClinVar
Risk rs113954997(G,T;G,T)
Alt rs113954997(G,T;G,T)
Reference rs113954997(A;A)
Significance Pathogenic
Disease Neoplasm of ovary
Variation info
Gene RRAS2
CLNDBN Neoplasm of ovary
Reversed 1
HGVS NC_000011.9:g.14316390T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010054.4,