rs121913373

Orientation

minus

Stabilized

minus

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

Make rs121913373(A;A)

Make rs121913373(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753321

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913373
dbSNP (classic)	rs121913373
ClinGen	rs121913373
ebi	rs121913373
HLI	rs121913373
Exac	rs121913373
Gnomad	rs121913373
Varsome	rs121913373
LitVar	rs121913373
Map	rs121913373
PheGenI	rs121913373
Biobank	rs121913373
1000 genomes	rs121913373
hgdp	rs121913373
ensembl	rs121913373
geneview	rs121913373
scholar	rs121913373
google	rs121913373
pharmgkb	rs121913373
gwascentral	rs121913373
openSNP	rs121913373
23andMe	rs121913373
SNPshot	rs121913373
SNPdbe	rs121913373
MSV3d	rs121913373
GWAS Ctlg	rs121913373

Max Magnitude

0

ClinVar
Risk	rs121913373(A;A)
Alt	rs121913373(A;A)
Reference	Rs121913373(G;G)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453121C>T
CLNSRC
CLNACC	RCV000437021.1,