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rs886039607

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039607(C;C)
Make rs886039607(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position12608842
GeneRAF1
is asnp
is mentioned by
dbSNPrs886039607
dbSNP (classic)rs886039607
ClinGenrs886039607
ebirs886039607
HLIrs886039607
Exacrs886039607
Gnomadrs886039607
Varsomers886039607
LitVarrs886039607
Maprs886039607
PheGenIrs886039607
Biobankrs886039607
1000 genomesrs886039607
hgdprs886039607
ensemblrs886039607
geneviewrs886039607
scholarrs886039607
googlers886039607
pharmgkbrs886039607
gwascentralrs886039607
openSNPrs886039607
23andMers886039607
SNPshotrs886039607
SNPdbers886039607
MSV3drs886039607
GWAS Ctlgrs886039607
Max Magnitude0
ClinVar
Risk rs886039607(C;C)
Alt rs886039607(C;C)
Reference Rs886039607(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.12650341C>G
CLNSRC
CLNACC RCV000255759.1,