rs1057517915

Orientation

minus

Stabilized

minus

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

Make rs1057517915(G;T)

Make rs1057517915(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140754202

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs1057517915
dbSNP (classic)	rs1057517915
ClinGen	rs1057517915
ebi	rs1057517915
HLI	rs1057517915
Exac	rs1057517915
Gnomad	rs1057517915
Varsome	rs1057517915
LitVar	rs1057517915
Map	rs1057517915
PheGenI	rs1057517915
Biobank	rs1057517915
1000 genomes	rs1057517915
hgdp	rs1057517915
ensembl	rs1057517915
geneview	rs1057517915
scholar	rs1057517915
google	rs1057517915
pharmgkb	rs1057517915
gwascentral	rs1057517915
openSNP	rs1057517915
23andMe	rs1057517915
SNPshot	rs1057517915
SNPdbe	rs1057517915
MSV3d	rs1057517915
GWAS Ctlg	rs1057517915

Max Magnitude

0

ClinVar
Risk	rs1057517915(T;T)
Alt	rs1057517915(T;T)
Reference	Rs1057517915(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	BRAF
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.140454002C>A
CLNSRC
CLNACC	RCV000413723.1,