rs121913372

Orientation

minus

Stabilized

minus

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

Make rs121913372(AG;TT)

Make rs121913372(TT;TT)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753321

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913372
dbSNP (classic)	rs121913372
ClinGen	rs121913372
ebi	rs121913372
HLI	rs121913372
Exac	rs121913372
Gnomad	rs121913372
Varsome	rs121913372
LitVar	rs121913372
Map	rs121913372
PheGenI	rs121913372
Biobank	rs121913372
1000 genomes	rs121913372
hgdp	rs121913372
ensembl	rs121913372
geneview	rs121913372
scholar	rs121913372
google	rs121913372
pharmgkb	rs121913372
gwascentral	rs121913372
openSNP	rs121913372
23andMe	rs121913372
SNPshot	rs121913372
SNPdbe	rs121913372
MSV3d	rs121913372
GWAS Ctlg	rs121913372

Max Magnitude

0

ClinVar
Risk	rs121913372(TT;TT)
Alt	rs121913372(TT;TT)
Reference	Rs121913372(AG;AG)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453121_140453122delCTinsAA
CLNSRC
CLNACC	RCV000419349.1,