rs1057519718

Orientation

minus

Stabilized

minus

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

Make rs1057519718(GA;GA)

Make rs1057519718(GA;TG)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753355

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs1057519718
dbSNP (classic)	rs1057519718
ClinGen	rs1057519718
ebi	rs1057519718
HLI	rs1057519718
Exac	rs1057519718
Gnomad	rs1057519718
Varsome	rs1057519718
LitVar	rs1057519718
Map	rs1057519718
PheGenI	rs1057519718
Biobank	rs1057519718
1000 genomes	rs1057519718
hgdp	rs1057519718
ensembl	rs1057519718
geneview	rs1057519718
scholar	rs1057519718
google	rs1057519718
pharmgkb	rs1057519718
gwascentral	rs1057519718
openSNP	rs1057519718
23andMe	rs1057519718
SNPshot	rs1057519718
SNPdbe	rs1057519718
MSV3d	rs1057519718
GWAS Ctlg	rs1057519718

Max Magnitude

0

ClinVar
Risk	rs1057519718(GA;GA)
Alt	rs1057519718(GA;GA)
Reference	Rs1057519718(TG;TG)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000007.13:g.140453155_140453156delCAinsTC
CLNSRC
CLNACC	RCV000427497.1,