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rs121913341

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913341(G;G)
Make rs121913341(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position140753350
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913341
ebirs121913341
HLIrs121913341
Exacrs121913341
Varsomers121913341
Maprs121913341
PheGenIrs121913341
hapmaprs121913341
1000 genomesrs121913341
hgdprs121913341
ensemblrs121913341
gopubmedrs121913341
geneviewrs121913341
scholarrs121913341
googlers121913341
pharmgkbrs121913341
gwascentralrs121913341
openSNPrs121913341
23andMers121913341
23andMe allrs121913341
SNP Nexus

SNPshotrs121913341
SNPdbers121913341
MSV3drs121913341
GWAS Ctlgrs121913341
Max Magnitude0
ClinVar
Risk rs121913341(A,G;A,G)
Alt rs121913341(A,G;A,G)
Reference rs121913341(T;T)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome not provided
Variation info
Gene BRAF
CLNDBN Cardiofaciocutaneous syndrome not provided
Reversed 1
HGVS NC_000007.13:g.140453150A>C; NC_000007.13:g.140453150A>T
CLNSRC
CLNACC RCV000154266.1, RCV000157825.2, RCV000157824.1,