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rs730881009

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881009(A;C)
Make rs730881009(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12609238
GeneRAF1
is asnp
is mentioned by
dbSNPrs730881009
ebirs730881009
HLIrs730881009
Exacrs730881009
Varsomers730881009
Maprs730881009
PheGenIrs730881009
hapmaprs730881009
1000 genomesrs730881009
hgdprs730881009
ensemblrs730881009
gopubmedrs730881009
geneviewrs730881009
scholarrs730881009
googlers730881009
pharmgkbrs730881009
gwascentralrs730881009
openSNPrs730881009
23andMers730881009
23andMe allrs730881009
SNP Nexus

SNPshotrs730881009
SNPdbers730881009
MSV3drs730881009
GWAS Ctlgrs730881009
Max Magnitude0
ClinVar
Risk rs730881009(C;C)
Alt rs730881009(C;C)
Reference rs730881009(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.12650737T>G
CLNSRC
CLNACC RCV000159094.1,