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rs730880965

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880965(A;A)
Make rs730880965(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position114713915
GeneNRAS
is asnp
is mentioned by
dbSNPrs730880965
ebirs730880965
HLIrs730880965
Exacrs730880965
Varsomers730880965
Maprs730880965
PheGenIrs730880965
hapmaprs730880965
1000 genomesrs730880965
hgdprs730880965
ensemblrs730880965
gopubmedrs730880965
geneviewrs730880965
scholarrs730880965
googlers730880965
pharmgkbrs730880965
gwascentralrs730880965
openSNPrs730880965
23andMers730880965
23andMe allrs730880965
SNP Nexus

SNPshotrs730880965
SNPdbers730880965
MSV3drs730880965
GWAS Ctlgrs730880965
Max Magnitude0
ClinVar
Risk rs730880965(A;A)
Alt rs730880965(A;A)
Reference rs730880965(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NRAS
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.115256536C>T
CLNSRC
CLNACC RCV000158981.1,