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rs730880469

From SNPedia

Orientationminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs730880469(-;-)
Make rs730880469(-;GAG)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position25227335
GeneKRAS
is asnp
is mentioned by
dbSNPrs730880469
ebirs730880469
HLIrs730880469
Exacrs730880469
Varsomers730880469
Maprs730880469
PheGenIrs730880469
hapmaprs730880469
1000 genomesrs730880469
hgdprs730880469
ensemblrs730880469
gopubmedrs730880469
geneviewrs730880469
scholarrs730880469
googlers730880469
pharmgkbrs730880469
gwascentralrs730880469
openSNPrs730880469
23andMers730880469
23andMe allrs730880469
SNP Nexus

SNPshotrs730880469
SNPdbers730880469
MSV3drs730880469
GWAS Ctlgrs730880469
Max Magnitude0
ClinVar
Risk rs730880469(;)
Alt rs730880469(;)
Reference rs730880469(GAG;GAG)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene KRAS
CLNDBN Rasopathy
Reversed 1
HGVS NC_000012.11:g.25380269_25380271delCTC
CLNSRC
CLNACC RCV000157931.1,