rs1057518105

Orientation

minus

Stabilized

minus

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

Make rs1057518105(C;C)

Make rs1057518105(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140801446

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs1057518105
dbSNP (classic)	rs1057518105
ClinGen	rs1057518105
ebi	rs1057518105
HLI	rs1057518105
Exac	rs1057518105
Gnomad	rs1057518105
Varsome	rs1057518105
LitVar	rs1057518105
Map	rs1057518105
PheGenI	rs1057518105
Biobank	rs1057518105
1000 genomes	rs1057518105
hgdp	rs1057518105
ensembl	rs1057518105
geneview	rs1057518105
scholar	rs1057518105
google	rs1057518105
pharmgkb	rs1057518105
gwascentral	rs1057518105
openSNP	rs1057518105
23andMe	rs1057518105
SNPshot	rs1057518105
SNPdbe	rs1057518105
MSV3d	rs1057518105
GWAS Ctlg	rs1057518105

Max Magnitude

0

ClinVar
Risk	rs1057518105(C;C)
Alt	rs1057518105(C;C)
Reference	Rs1057518105(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	BRAF
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.140501246C>G
CLNSRC
CLNACC	RCV000414050.1,