rs121913366

Orientation

minus

Stabilized

minus

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

Make rs121913366(A;A)

Make rs121913366(A;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140753345

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913366
dbSNP (classic)	rs121913366
ClinGen	rs121913366
ebi	rs121913366
HLI	rs121913366
Exac	rs121913366
Gnomad	rs121913366
Varsome	rs121913366
LitVar	rs121913366
Map	rs121913366
PheGenI	rs121913366
Biobank	rs121913366
1000 genomes	rs121913366
hgdp	rs121913366
ensembl	rs121913366
geneview	rs121913366
scholar	rs121913366
google	rs121913366
pharmgkb	rs121913366
gwascentral	rs121913366
openSNP	rs121913366
23andMe	rs121913366
SNPshot	rs121913366
SNPdbe	rs121913366
MSV3d	rs121913366
GWAS Ctlg	rs121913366

Max Magnitude

0

OMIM	164757
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121913366(A;A) rs121913366(G;G)
Alt	rs121913366(A;A) rs121913366(G;G)
Reference	Rs121913366(T;T)
Significance	Pathogenic
Disease	Adenocarcinoma of lung Adenocarcinoma of prostate Malignant melanoma of skin Multiple myeloma Malignant melanoma Ovarian Neoplasms
Variation	info
Gene	BRAF
CLNDBN	Adenocarcinoma of lung Adenocarcinoma of prostate Malignant melanoma of skin Multiple myeloma Malignant melanoma Ovarian Neoplasms
Reversed	1
HGVS	NC_000007.13:g.140453145A>C; NC_000007.13:g.140453145A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015002.5, RCV000421201.1, RCV000421775.1, RCV000432024.1, RCV000439504.1, RCV000444137.1, RCV000427485.1, RCV000431444.1, RCV000437736.1, RCV000443326.1,