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rs1057519720

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs1057519720(GG;TT)
Make rs1057519720(TT;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140781602
GeneBRAF
is asnp
is mentioned by
dbSNPrs1057519720
dbSNP (old)rs1057519720
ClinGenrs1057519720
ebirs1057519720
HLIrs1057519720
Exacrs1057519720
Gnomadrs1057519720
Varsomers1057519720
LitVarrs1057519720
Maprs1057519720
PheGenIrs1057519720
Biobankrs1057519720
1000 genomesrs1057519720
hgdprs1057519720
ensemblrs1057519720
gopubmedrs1057519720
geneviewrs1057519720
scholarrs1057519720
googlers1057519720
pharmgkbrs1057519720
gwascentralrs1057519720
openSNPrs1057519720
23andMers1057519720
23andMe allrs1057519720
SNPshotrs1057519720
SNPdbers1057519720
MSV3drs1057519720
GWAS Ctlgrs1057519720
Max Magnitude0
ClinVar
Risk rs1057519720(TC;TC) rs1057519720(TT;TT)
Alt rs1057519720(TC;TC) rs1057519720(TT;TT)
Reference Rs1057519720(GG;GG)
Significance Pathogenic
Disease Lung cancer Malignant melanoma
Variation info
Gene BRAF
CLNDBN Lung cancer Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140481402_140481403delCCinsAA; NC_000007.13:g.140481402_140481403delCCinsGA
CLNSRC
CLNACC RCV000429405.1, RCV000421677.1,