rs121913337

Orientation

minus

Stabilized

minus

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

Make rs121913337(A;A)

Make rs121913337(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753353

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913337
dbSNP (classic)	rs121913337
ClinGen	rs121913337
ebi	rs121913337
HLI	rs121913337
Exac	rs121913337
Gnomad	rs121913337
Varsome	rs121913337
LitVar	rs121913337
Map	rs121913337
PheGenI	rs121913337
Biobank	rs121913337
1000 genomes	rs121913337
hgdp	rs121913337
ensembl	rs121913337
geneview	rs121913337
scholar	rs121913337
google	rs121913337
pharmgkb	rs121913337
gwascentral	rs121913337
openSNP	rs121913337
23andMe	rs121913337
SNPshot	rs121913337
SNPdbe	rs121913337
MSV3d	rs121913337
GWAS Ctlg	rs121913337

Max Magnitude

0

ClinVar
Risk	rs121913337(A;A) rs121913337(G;G)
Alt	rs121913337(A;A) rs121913337(G;G)
Reference	Rs121913337(T;T)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453153A>C; NC_000007.13:g.140453153A>T
CLNSRC
CLNACC	RCV000428481.1, RCV000438728.1,