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rs121913377

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs121913377(AT;AT)
Make rs121913377(AT;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753335
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913377
dbSNP (old)rs121913377
ClinGenrs121913377
ebirs121913377
HLIrs121913377
Exacrs121913377
Gnomadrs121913377
Varsomers121913377
Maprs121913377
PheGenIrs121913377
Biobankrs121913377
1000 genomesrs121913377
hgdprs121913377
ensemblrs121913377
gopubmedrs121913377
geneviewrs121913377
scholarrs121913377
googlers121913377
pharmgkbrs121913377
gwascentralrs121913377
openSNPrs121913377
23andMers121913377
23andMe allrs121913377
SNPshotrs121913377
SNPdbers121913377
MSV3drs121913377
GWAS Ctlgrs121913377
Max Magnitude0
ClinVar
Risk rs121913377(AA;AA) rs121913377(AT;AT)
Alt rs121913377(AA;AA) rs121913377(AT;AT)
Reference Rs121913377(TG;TG)
Significance Pathogenic
Disease Malignant melanoma Colonic Neoplasms
Variation info
Gene BRAF
CLNDBN Malignant melanoma Colonic Neoplasms
Reversed 1
HGVS NC_000007.13:g.140453135_140453136delCAinsAT; NC_000007.13:g.140453135_140453136delCAinsTT
CLNSRC
CLNACC RCV000423512.1, RCV000424781.1, RCV000442563.1,