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rs730880382

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880382(G;T)
Make rs730880382(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12591708
GeneRAF1
is asnp
is mentioned by
dbSNPrs730880382
ebirs730880382
HLIrs730880382
Exacrs730880382
Varsomers730880382
Maprs730880382
PheGenIrs730880382
hapmaprs730880382
1000 genomesrs730880382
hgdprs730880382
ensemblrs730880382
gopubmedrs730880382
geneviewrs730880382
scholarrs730880382
googlers730880382
pharmgkbrs730880382
gwascentralrs730880382
openSNPrs730880382
23andMers730880382
23andMe allrs730880382
SNP Nexus

SNPshotrs730880382
SNPdbers730880382
MSV3drs730880382
GWAS Ctlgrs730880382
Max Magnitude0
ClinVar
Risk rs730880382(T;T)
Alt rs730880382(T;T)
Reference rs730880382(G;G)
Significance Probable-Pathogenic
Disease not provided Rasopathy
Variation info
Gene RAF1
CLNDBN not provided Rasopathy
Reversed 1
HGVS NC_000003.11:g.12633207C>A
CLNSRC
CLNACC RCV000157687.1, RCV000159082.1,