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rs730881002

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881002(A;G)
Make rs730881002(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12590889
GeneRAF1
is asnp
is mentioned by
dbSNPrs730881002
ebirs730881002
HLIrs730881002
Exacrs730881002
Varsomers730881002
Maprs730881002
PheGenIrs730881002
hapmaprs730881002
1000 genomesrs730881002
hgdprs730881002
ensemblrs730881002
gopubmedrs730881002
geneviewrs730881002
scholarrs730881002
googlers730881002
pharmgkbrs730881002
gwascentralrs730881002
openSNPrs730881002
23andMers730881002
23andMe allrs730881002
SNP Nexus

SNPshotrs730881002
SNPdbers730881002
MSV3drs730881002
GWAS Ctlgrs730881002
Max Magnitude0
ClinVar
Risk rs730881002(G;G)
Alt rs730881002(G;G)
Reference rs730881002(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RAF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.12632388T>C
CLNSRC
CLNACC RCV000159084.1,