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rs121913368

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs121913368(CT;TC)
Make rs121913368(TC;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753345
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913368
dbSNP (classic)rs121913368
ClinGenrs121913368
ebirs121913368
HLIrs121913368
Exacrs121913368
Gnomadrs121913368
Varsomers121913368
LitVarrs121913368
Maprs121913368
PheGenIrs121913368
Biobankrs121913368
1000 genomesrs121913368
hgdprs121913368
ensemblrs121913368
geneviewrs121913368
scholarrs121913368
googlers121913368
pharmgkbrs121913368
gwascentralrs121913368
openSNPrs121913368
23andMers121913368
23andMe allrs121913368
SNPshotrs121913368
SNPdbers121913368
MSV3drs121913368
GWAS Ctlgrs121913368
Max Magnitude0
ClinVar
Risk rs121913368(TC;TC)
Alt rs121913368(TC;TC)
Reference Rs121913368(CT;CT)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene BRAF
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140453145_140453146delAGinsGA
CLNSRC
CLNACC RCV000443303.1,