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rs121913365

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913365(A;C)
Make rs121913365(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753332
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913365
dbSNP (old)rs121913365
ClinGenrs121913365
ebirs121913365
HLIrs121913365
Exacrs121913365
Gnomadrs121913365
Varsomers121913365
Maprs121913365
PheGenIrs121913365
Biobankrs121913365
1000 genomesrs121913365
hgdprs121913365
ensemblrs121913365
gopubmedrs121913365
geneviewrs121913365
scholarrs121913365
googlers121913365
pharmgkbrs121913365
gwascentralrs121913365
openSNPrs121913365
23andMers121913365
23andMe allrs121913365
SNPshotrs121913365
SNPdbers121913365
MSV3drs121913365
GWAS Ctlgrs121913365
Max Magnitude0
ClinVar
Risk rs121913365(C;C) rs121913365(T;T)
Alt rs121913365(C;C) rs121913365(T;T)
Reference Rs121913365(A;A)
Significance Probable-Pathogenic
Disease Malignant melanoma Malignant melanoma of skin Chronic lymphocytic leukemia Adenocarcinoma of prostate Neoplasm of the thyroid gland Adenocarcinoma of stomach Adenocarcinoma of lung Malignant neoplasm of body of uterus
Variation info
Gene BRAF
CLNDBN Malignant melanoma Malignant melanoma of skin Chronic lymphocytic leukemia Adenocarcinoma of prostate Neoplasm of the thyroid gland Adenocarcinoma of stomach Adenocarcinoma of lung Malignant neoplasm of body of uterus
Reversed 1
HGVS NC_000007.13:g.140453132T>A; NC_000007.13:g.140453132T>G
CLNSRC
CLNACC RCV000430483.1, RCV000420022.1, RCV000421086.1, RCV000421724.1, RCV000428269.1, RCV000431157.1, RCV000438949.1, RCV000441196.1, RCV000441430.1,