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rs730881003

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881003(C;C)
Make rs730881003(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12585794
GeneRAF1
is asnp
is mentioned by
dbSNPrs730881003
ebirs730881003
HLIrs730881003
Exacrs730881003
Varsomers730881003
Maprs730881003
PheGenIrs730881003
hapmaprs730881003
1000 genomesrs730881003
hgdprs730881003
ensemblrs730881003
gopubmedrs730881003
geneviewrs730881003
scholarrs730881003
googlers730881003
pharmgkbrs730881003
gwascentralrs730881003
openSNPrs730881003
23andMers730881003
23andMe allrs730881003
SNP Nexus

SNPshotrs730881003
SNPdbers730881003
MSV3drs730881003
GWAS Ctlgrs730881003
Max Magnitude0
ClinVar
Risk rs730881003(C;C)
Alt rs730881003(C;C)
Reference rs730881003(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RAF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.12627293A>G
CLNSRC
CLNACC RCV000159085.1,