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rs1057517813

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517813(G;G)
Make rs1057517813(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position12608864
GeneRAF1
is asnp
is mentioned by
dbSNPrs1057517813
dbSNP (old)rs1057517813
ClinGenrs1057517813
ebirs1057517813
HLIrs1057517813
Exacrs1057517813
Gnomadrs1057517813
Varsomers1057517813
Maprs1057517813
PheGenIrs1057517813
Biobankrs1057517813
1000 genomesrs1057517813
hgdprs1057517813
ensemblrs1057517813
gopubmedrs1057517813
geneviewrs1057517813
scholarrs1057517813
googlers1057517813
pharmgkbrs1057517813
gwascentralrs1057517813
openSNPrs1057517813
23andMers1057517813
23andMe allrs1057517813
SNPshotrs1057517813
SNPdbers1057517813
MSV3drs1057517813
GWAS Ctlgrs1057517813
Max Magnitude0
ClinVar
Risk rs1057517813(G;G)
Alt rs1057517813(G;G)
Reference Rs1057517813(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.12650363A>C
CLNSRC
CLNACC RCV000412745.1,