rs121913226

Orientation

minus

Stabilized

minus

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

Make rs121913226(-;-)

Make rs121913226(-;AAA)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753332

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913226
dbSNP (classic)	rs121913226
ClinGen	rs121913226
ebi	rs121913226
HLI	rs121913226
Exac	rs121913226
Gnomad	rs121913226
Varsome	rs121913226
LitVar	rs121913226
Map	rs121913226
PheGenI	rs121913226
Biobank	rs121913226
1000 genomes	rs121913226
hgdp	rs121913226
ensembl	rs121913226
geneview	rs121913226
scholar	rs121913226
google	rs121913226
pharmgkb	rs121913226
gwascentral	rs121913226
openSNP	rs121913226
23andMe	rs121913226
SNPshot	rs121913226
SNPdbe	rs121913226
MSV3d	rs121913226
GWAS Ctlg	rs121913226

Max Magnitude

0

ClinVar
Risk	rs121913226(-;-)
Alt	rs121913226(-;-)
Reference	Rs121913226(AAA;AAA)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453132_140453134delTTT
CLNSRC
CLNACC	RCV000432391.1,