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rs121913226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAA;AAA) 0 common in clinvar
Make rs121913226(-;-)
Make rs121913226(-;AAA)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753332
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913226
dbSNP (old)rs121913226
ClinGenrs121913226
ebirs121913226
HLIrs121913226
Exacrs121913226
Gnomadrs121913226
Varsomers121913226
Maprs121913226
PheGenIrs121913226
Biobankrs121913226
1000 genomesrs121913226
hgdprs121913226
ensemblrs121913226
gopubmedrs121913226
geneviewrs121913226
scholarrs121913226
googlers121913226
pharmgkbrs121913226
gwascentralrs121913226
openSNPrs121913226
23andMers121913226
23andMe allrs121913226
SNPshotrs121913226
SNPdbers121913226
MSV3drs121913226
GWAS Ctlgrs121913226
Max Magnitude0
ClinVar
Risk rs121913226(-;-)
Alt rs121913226(-;-)
Reference Rs121913226(AAA;AAA)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene BRAF
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140453132_140453134delTTT
CLNSRC
CLNACC RCV000432391.1,