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rs121913357

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913357(A;A)
Make rs121913357(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140781603
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913357
ebirs121913357
HLIrs121913357
Exacrs121913357
Varsomers121913357
Maprs121913357
PheGenIrs121913357
hapmaprs121913357
1000 genomesrs121913357
hgdprs121913357
ensemblrs121913357
gopubmedrs121913357
geneviewrs121913357
scholarrs121913357
googlers121913357
pharmgkbrs121913357
gwascentralrs121913357
openSNPrs121913357
23andMers121913357
23andMe allrs121913357
SNP Nexus

SNPshotrs121913357
SNPdbers121913357
MSV3drs121913357
GWAS Ctlgrs121913357
Max Magnitude0
OMIM164757
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121913357(A,C,T;A,C,T)
Alt rs121913357(A,C,T;A,C,T)
Reference rs121913357(G;G)
Significance Pathogenic
Disease not specified Malignant lymphoma not provided Non-small cell lung cancer
Variation info
Gene BRAF
CLNDBN not specified Malignant lymphoma, non-Hodgkin not provided Non-small cell lung cancer
Reversed 1
HGVS NC_000007.13:g.140481403C>A; NC_000007.13:g.140481403C>G; NC_000007.13:g.140481403C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000150211.1, RCV000015004.8, RCV000033306.4, RCV000154398.1,