rs121913365

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs121913365(A;C)

Make rs121913365(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753332

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913365
dbSNP (classic)	rs121913365
ClinGen	rs121913365
ebi	rs121913365
HLI	rs121913365
Exac	rs121913365
Gnomad	rs121913365
Varsome	rs121913365
LitVar	rs121913365
Map	rs121913365
PheGenI	rs121913365
Biobank	rs121913365
1000 genomes	rs121913365
hgdp	rs121913365
ensembl	rs121913365
geneview	rs121913365
scholar	rs121913365
google	rs121913365
pharmgkb	rs121913365
gwascentral	rs121913365
openSNP	rs121913365
23andMe	rs121913365
SNPshot	rs121913365
SNPdbe	rs121913365
MSV3d	rs121913365
GWAS Ctlg	rs121913365

Max Magnitude

0

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,