Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057518155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518155(A;C)
Make rs1057518155(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position12608914
GeneRAF1
is asnp
is mentioned by
dbSNPrs1057518155
dbSNP (old)rs1057518155
ClinGenrs1057518155
ebirs1057518155
HLIrs1057518155
Exacrs1057518155
Gnomadrs1057518155
Varsomers1057518155
Maprs1057518155
PheGenIrs1057518155
Biobankrs1057518155
1000 genomesrs1057518155
hgdprs1057518155
ensemblrs1057518155
gopubmedrs1057518155
geneviewrs1057518155
scholarrs1057518155
googlers1057518155
pharmgkbrs1057518155
gwascentralrs1057518155
openSNPrs1057518155
23andMers1057518155
23andMe allrs1057518155
SNPshotrs1057518155
SNPdbers1057518155
MSV3drs1057518155
GWAS Ctlgrs1057518155
Max Magnitude0
ClinVar
Risk rs1057518155(C;C)
Alt rs1057518155(C;C)
Reference Rs1057518155(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.12650413T>G
CLNSRC
CLNACC RCV000414587.1,