Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913364

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913364(A;G)
Make rs121913364(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753334
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913364
ebirs121913364
HLIrs121913364
Exacrs121913364
Varsomers121913364
Maprs121913364
PheGenIrs121913364
hapmaprs121913364
1000 genomesrs121913364
hgdprs121913364
ensemblrs121913364
gopubmedrs121913364
geneviewrs121913364
scholarrs121913364
googlers121913364
pharmgkbrs121913364
gwascentralrs121913364
openSNPrs121913364
23andMers121913364
23andMe allrs121913364
SNP Nexus

SNPshotrs121913364
SNPdbers121913364
MSV3drs121913364
GWAS Ctlgrs121913364
Max Magnitude0
OMIM164757
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121913364(C,G;C,G)
Alt rs121913364(C,G;C,G)
Reference rs121913364(A;A)
Significance Pathogenic
Disease Carcinoma of colon Thyroid cancer Non-small cell lung cancer not provided Rasopathy
Variation info
Gene BRAF
CLNDBN Carcinoma of colon Thyroid cancer, follicular Non-small cell lung cancer not provided Rasopathy
Reversed 1
HGVS NC_000007.13:g.140453134T>C; NC_000007.13:g.140453134T>G
CLNSRC OMIM Allelic Variant HGMD
CLNACC RCV000014999.6, RCV000015000.6, RCV000037938.2, RCV000034332.5, RCV000150201.2,