rs121913363

Orientation

minus

Stabilized

minus

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

Make rs121913363(A;G)

Make rs121913363(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753361

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913363
dbSNP (classic)	rs121913363
ClinGen	rs121913363
ebi	rs121913363
HLI	rs121913363
Exac	rs121913363
Gnomad	rs121913363
Varsome	rs121913363
LitVar	rs121913363
Map	rs121913363
PheGenI	rs121913363
Biobank	rs121913363
1000 genomes	rs121913363
hgdp	rs121913363
ensembl	rs121913363
geneview	rs121913363
scholar	rs121913363
google	rs121913363
pharmgkb	rs121913363
gwascentral	rs121913363
openSNP	rs121913363
23andMe	rs121913363
SNPshot	rs121913363
SNPdbe	rs121913363
MSV3d	rs121913363
GWAS Ctlg	rs121913363

Max Magnitude

0

ClinVar
Risk	rs121913363(G;G)
Alt	rs121913363(G;G)
Reference	Rs121913363(A;A)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453161T>C
CLNSRC
CLNACC	RCV000427646.1,