rs121913368

Orientation

minus

Stabilized

minus

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

Make rs121913368(CT;TC)

Make rs121913368(TC;TC)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753345

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913368
dbSNP (classic)	rs121913368
ClinGen	rs121913368
ebi	rs121913368
HLI	rs121913368
Exac	rs121913368
Gnomad	rs121913368
Varsome	rs121913368
LitVar	rs121913368
Map	rs121913368
PheGenI	rs121913368
Biobank	rs121913368
1000 genomes	rs121913368
hgdp	rs121913368
ensembl	rs121913368
geneview	rs121913368
scholar	rs121913368
google	rs121913368
pharmgkb	rs121913368
gwascentral	rs121913368
openSNP	rs121913368
23andMe	rs121913368
SNPshot	rs121913368
SNPdbe	rs121913368
MSV3d	rs121913368
GWAS Ctlg	rs121913368

Max Magnitude

0

ClinVar
Risk	rs121913368(TC;TC)
Alt	rs121913368(TC;TC)
Reference	Rs121913368(CT;CT)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453145_140453146delAGinsGA
CLNSRC
CLNACC	RCV000443303.1,