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rs55939351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs55939351(A;T)
Make rs55939351(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753360
GeneBRAF
is asnp
is mentioned by
dbSNPrs55939351
ebirs55939351
HLIrs55939351
Exacrs55939351
Varsomers55939351
Maprs55939351
PheGenIrs55939351
hapmaprs55939351
1000 genomesrs55939351
hgdprs55939351
ensemblrs55939351
gopubmedrs55939351
geneviewrs55939351
scholarrs55939351
googlers55939351
pharmgkbrs55939351
gwascentralrs55939351
openSNPrs55939351
23andMers55939351
23andMe allrs55939351
SNP Nexus

SNPshotrs55939351
SNPdbers55939351
MSV3drs55939351
GWAS Ctlgrs55939351
Max Magnitude0
ClinVar
Risk rs55939351(G,T;G,T)
Alt rs55939351(G,T;G,T)
Reference rs55939351(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRAF
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.140453160A>G
CLNSRC ClinVar
CLNACC RCV000033331.3,