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rs1057518105

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518105(C;C)
Make rs1057518105(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140801446
GeneBRAF
is asnp
is mentioned by
dbSNPrs1057518105
dbSNP (old)rs1057518105
ClinGenrs1057518105
ebirs1057518105
HLIrs1057518105
Exacrs1057518105
Gnomadrs1057518105
Varsomers1057518105
Maprs1057518105
PheGenIrs1057518105
Biobankrs1057518105
1000 genomesrs1057518105
hgdprs1057518105
ensemblrs1057518105
gopubmedrs1057518105
geneviewrs1057518105
scholarrs1057518105
googlers1057518105
pharmgkbrs1057518105
gwascentralrs1057518105
openSNPrs1057518105
23andMers1057518105
23andMe allrs1057518105
SNPshotrs1057518105
SNPdbers1057518105
MSV3drs1057518105
GWAS Ctlgrs1057518105
Max Magnitude0
ClinVar
Risk rs1057518105(C;C)
Alt rs1057518105(C;C)
Reference Rs1057518105(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRAF
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.140501246C>G
CLNSRC
CLNACC RCV000414050.1,