rs121913340

Orientation

minus

Stabilized

minus

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

Make rs121913340(A;A)

Make rs121913340(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753379

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913340
dbSNP (classic)	rs121913340
ClinGen	rs121913340
ebi	rs121913340
HLI	rs121913340
Exac	rs121913340
Gnomad	rs121913340
Varsome	rs121913340
LitVar	rs121913340
Map	rs121913340
PheGenI	rs121913340
Biobank	rs121913340
1000 genomes	rs121913340
hgdp	rs121913340
ensembl	rs121913340
geneview	rs121913340
scholar	rs121913340
google	rs121913340
pharmgkb	rs121913340
gwascentral	rs121913340
openSNP	rs121913340
23andMe	rs121913340
SNPshot	rs121913340
SNPdbe	rs121913340
MSV3d	rs121913340
GWAS Ctlg	rs121913340

Max Magnitude

0

ClinVar
Risk	rs121913340(A;A)
Alt	rs121913340(A;A)
Reference	Rs121913340(G;G)
Significance	Probable-Pathogenic
Disease	not specified Malignant melanoma Neoplasm
Variation	info
Gene	BRAF
CLNDBN	not specified Malignant melanoma Neoplasm
Reversed	1
HGVS	NC_000007.13:g.140453179C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000037930.2, RCV000419782.1, RCV000437874.1,