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rs397516890

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGA;GGA) 0 common in clinvar
Make rs397516890(-;-)
Make rs397516890(-;GGA)
ReferenceGRCh38 38.1/141
Chromosome7
Position140781601
GeneBRAF
is asnp
is mentioned by
dbSNPrs397516890
ebirs397516890
HLIrs397516890
Exacrs397516890
Varsomers397516890
Maprs397516890
PheGenIrs397516890
hapmaprs397516890
1000 genomesrs397516890
hgdprs397516890
ensemblrs397516890
gopubmedrs397516890
geneviewrs397516890
scholarrs397516890
googlers397516890
pharmgkbrs397516890
gwascentralrs397516890
openSNPrs397516890
23andMers397516890
23andMe allrs397516890
SNP Nexus

SNPshotrs397516890
SNPdbers397516890
MSV3drs397516890
GWAS Ctlgrs397516890
Max Magnitude0
ClinVar
Risk rs397516890(;)
Alt rs397516890(;)
Reference rs397516890(GGA;GGA)
Significance Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene BRAF
CLNDBN Non-small cell lung cancer
Reversed 1
HGVS NC_000007.13:g.140481401_140481403delTCC
CLNSRC ClinVar
CLNACC RCV000037918.2,