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rs869025340

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025340(C;C)
Make rs869025340(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position140777032
GeneBRAF
is asnp
is mentioned by
dbSNPrs869025340
ebirs869025340
HLIrs869025340
Exacrs869025340
Varsomers869025340
Maprs869025340
PheGenIrs869025340
hapmaprs869025340
1000 genomesrs869025340
hgdprs869025340
ensemblrs869025340
gopubmedrs869025340
geneviewrs869025340
scholarrs869025340
googlers869025340
pharmgkbrs869025340
gwascentralrs869025340
openSNPrs869025340
23andMers869025340
23andMe allrs869025340
SNP Nexus

SNPshotrs869025340
SNPdbers869025340
MSV3drs869025340
GWAS Ctlgrs869025340
Max Magnitude0
ClinVar
Risk rs869025340(C;C)
Alt rs869025340(C;C)
Reference rs869025340(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRAF
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.140476832A>G
CLNSRC
CLNACC RCV000207510.1,