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rs730880967

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880967(-;-)
Make rs730880967(-;GGA)
Make rs730880967(GGA;GGA)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position114713976
GeneNRAS
is asnp
is mentioned by
dbSNPrs730880967
ebirs730880967
HLIrs730880967
Exacrs730880967
Varsomers730880967
Maprs730880967
PheGenIrs730880967
hapmaprs730880967
1000 genomesrs730880967
hgdprs730880967
ensemblrs730880967
gopubmedrs730880967
geneviewrs730880967
scholarrs730880967
googlers730880967
pharmgkbrs730880967
gwascentralrs730880967
openSNPrs730880967
23andMers730880967
23andMe allrs730880967
SNP Nexus

SNPshotrs730880967
SNPdbers730880967
MSV3drs730880967
GWAS Ctlgrs730880967
Max Magnitude0
ClinVar
Risk rs730880967(GGA;GGA)
Alt rs730880967(GGA;GGA)
Reference rs730880967(;)
Significance Pathogenic
Disease Rasopathy
Variation info
Gene NRAS
CLNDBN Rasopathy
Reversed 1
HGVS NC_000001.10:g.115256598_115256600dupTCC
CLNSRC
CLNACC RCV000158984.1,