rs121913371

Orientation

minus

Stabilized

minus

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

Make rs121913371(C;T)

Make rs121913371(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140781678

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913371
dbSNP (classic)	rs121913371
ClinGen	rs121913371
ebi	rs121913371
HLI	rs121913371
Exac	rs121913371
Gnomad	rs121913371
Varsome	rs121913371
LitVar	rs121913371
Map	rs121913371
PheGenI	rs121913371
Biobank	rs121913371
1000 genomes	rs121913371
hgdp	rs121913371
ensembl	rs121913371
geneview	rs121913371
scholar	rs121913371
google	rs121913371
pharmgkb	rs121913371
gwascentral	rs121913371
openSNP	rs121913371
23andMe	rs121913371
SNPshot	rs121913371
SNPdbe	rs121913371
MSV3d	rs121913371
GWAS Ctlg	rs121913371

Max Magnitude

0

ClinVar
Risk	rs121913371(A;A) rs121913371(T;T)
Alt	rs121913371(A;A) rs121913371(T;T)
Reference	Rs121913371(C;C)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140481478G>A
CLNSRC
CLNACC	RCV000435724.1,