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rs1057519719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519719(A;G)
Make rs1057519719(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140781593
GeneBRAF
is asnp
is mentioned by
dbSNPrs1057519719
dbSNP (old)rs1057519719
ClinGenrs1057519719
ebirs1057519719
HLIrs1057519719
Exacrs1057519719
Gnomadrs1057519719
Varsomers1057519719
LitVarrs1057519719
Maprs1057519719
PheGenIrs1057519719
Biobankrs1057519719
1000 genomesrs1057519719
hgdprs1057519719
ensemblrs1057519719
gopubmedrs1057519719
geneviewrs1057519719
scholarrs1057519719
googlers1057519719
pharmgkbrs1057519719
gwascentralrs1057519719
openSNPrs1057519719
23andMers1057519719
23andMe allrs1057519719
SNPshotrs1057519719
SNPdbers1057519719
MSV3drs1057519719
GWAS Ctlgrs1057519719
Max Magnitude0
ClinVar
Risk rs1057519719(G;G)
Alt rs1057519719(G;G)
Reference Rs1057519719(A;A)
Significance Pathogenic
Disease Lung cancer
Variation info
Gene BRAF
CLNDBN Lung cancer
Reversed 1
HGVS NC_000007.13:g.140481393T>C
CLNSRC
CLNACC RCV000438175.1,