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rs730881004

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881004(C;T)
Make rs730881004(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12584647
GeneRAF1
is asnp
is mentioned by
dbSNPrs730881004
ebirs730881004
HLIrs730881004
Exacrs730881004
Varsomers730881004
Maprs730881004
PheGenIrs730881004
hapmaprs730881004
1000 genomesrs730881004
hgdprs730881004
ensemblrs730881004
gopubmedrs730881004
geneviewrs730881004
scholarrs730881004
googlers730881004
pharmgkbrs730881004
gwascentralrs730881004
openSNPrs730881004
23andMers730881004
23andMe allrs730881004
SNP Nexus

SNPshotrs730881004
SNPdbers730881004
MSV3drs730881004
GWAS Ctlgrs730881004
Max Magnitude0
ClinVar
Risk rs730881004(T;T)
Alt rs730881004(T;T)
Reference rs730881004(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.12626146G>A
CLNSRC
CLNACC RCV000159088.2,