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rs397516903

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516903(G;G)
Make rs397516903(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position140801533
GeneBRAF
is asnp
is mentioned by
dbSNPrs397516903
ebirs397516903
HLIrs397516903
Exacrs397516903
Varsomers397516903
Maprs397516903
PheGenIrs397516903
hapmaprs397516903
1000 genomesrs397516903
hgdprs397516903
ensemblrs397516903
gopubmedrs397516903
geneviewrs397516903
scholarrs397516903
googlers397516903
pharmgkbrs397516903
gwascentralrs397516903
openSNPrs397516903
23andMers397516903
23andMe allrs397516903
SNP Nexus

SNPshotrs397516903
SNPdbers397516903
MSV3drs397516903
GWAS Ctlgrs397516903
Max Magnitude0
ClinVar
Risk rs397516903(C,G;C,G)
Alt rs397516903(C,G;C,G)
Reference rs397516903(T;T)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene BRAF
CLNDBN not specified not provided
Reversed 1
HGVS NC_000007.13:g.140501333A>C; NC_000007.13:g.140501333A>G
CLNSRC
CLNACC RCV000037958.2, RCV000157818.2,