rs121913361

Orientation

minus

Stabilized

minus

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

Make rs121913361(C;C)

Make rs121913361(C;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140753349

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913361
dbSNP (classic)	rs121913361
ClinGen	rs121913361
ebi	rs121913361
HLI	rs121913361
Exac	rs121913361
Gnomad	rs121913361
Varsome	rs121913361
LitVar	rs121913361
Map	rs121913361
PheGenI	rs121913361
Biobank	rs121913361
1000 genomes	rs121913361
hgdp	rs121913361
ensembl	rs121913361
geneview	rs121913361
scholar	rs121913361
google	rs121913361
pharmgkb	rs121913361
gwascentral	rs121913361
openSNP	rs121913361
23andMe	rs121913361
SNPshot	rs121913361
SNPdbe	rs121913361
MSV3d	rs121913361
GWAS Ctlg	rs121913361

Max Magnitude

0

ClinVar
Risk	rs121913361(A;A) rs121913361(C;C) rs121913361(T;T)
Alt	rs121913361(A;A) rs121913361(C;C) rs121913361(T;T)
Reference	Rs121913361(G;G)
Significance	Pathogenic
Disease	not specified Adenocarcinoma of lung Malignant melanoma Multiple myeloma Colorectal Neoplasms Transitional cell carcinoma of the bladder Glioblastoma
Variation	info
Gene	BRAF
CLNDBN	not specified Adenocarcinoma of lung Malignant melanoma Multiple myeloma Colorectal Neoplasms Transitional cell carcinoma of the bladder Glioblastoma
Reversed	1
HGVS	NC_000007.13:g.140453149C>A; NC_000007.13:g.140453149C>G; NC_000007.13:g.140453149C>T
CLNSRC	ClinVar
CLNACC	RCV000037933.4, RCV000418853.1, RCV000421748.1, RCV000429106.1, RCV000429746.1, RCV000436498.1, RCV000439396.1, RCV000422893.1, RCV000423119.1, RCV000433824.1, RCV000442552.1,