rs121913378

Orientation

minus

Stabilized

minus

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

Make rs121913378(G;T)

Make rs121913378(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140753337

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913378
dbSNP (classic)	rs121913378
ClinGen	rs121913378
ebi	rs121913378
HLI	rs121913378
Exac	rs121913378
Gnomad	rs121913378
Varsome	rs121913378
LitVar	rs121913378
Map	rs121913378
PheGenI	rs121913378
Biobank	rs121913378
1000 genomes	rs121913378
hgdp	rs121913378
ensembl	rs121913378
geneview	rs121913378
scholar	rs121913378
google	rs121913378
pharmgkb	rs121913378
gwascentral	rs121913378
openSNP	rs121913378
23andMe	rs121913378
SNPshot	rs121913378
SNPdbe	rs121913378
MSV3d	rs121913378
GWAS Ctlg	rs121913378

Max Magnitude

0

ClinVar
Risk	rs121913378(A;A) rs121913378(C;C) rs121913378(T;T)
Alt	rs121913378(A;A) rs121913378(C;C) rs121913378(T;T)
Reference	Rs121913378(G;G)
Significance	Pathogenic
Disease	Non-small cell lung cancer Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Non-small cell lung cancer Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453137C>A; NC_000007.13:g.140453137C>G; NC_000007.13:g.140453137C>T
CLNSRC	ClinVar
CLNACC	RCV000037935.2, RCV000435048.1, RCV000422356.1, RCV000037934.2, RCV000429286.1,