rs121913225

Orientation

minus

Stabilized

minus

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

Make rs121913225(C;C)

Make rs121913225(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753351

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913225
dbSNP (classic)	rs121913225
ClinGen	rs121913225
ebi	rs121913225
HLI	rs121913225
Exac	rs121913225
Gnomad	rs121913225
Varsome	rs121913225
LitVar	rs121913225
Map	rs121913225
PheGenI	rs121913225
Biobank	rs121913225
1000 genomes	rs121913225
hgdp	rs121913225
ensembl	rs121913225
geneview	rs121913225
scholar	rs121913225
google	rs121913225
pharmgkb	rs121913225
gwascentral	rs121913225
openSNP	rs121913225
23andMe	rs121913225
SNPshot	rs121913225
SNPdbe	rs121913225
MSV3d	rs121913225
GWAS Ctlg	rs121913225

Max Magnitude

0

ClinVar
Risk	rs121913225(C;C)
Alt	rs121913225(C;C)
Reference	Rs121913225(T;T)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453151A>G
CLNSRC
CLNACC	RCV000444314.1,