rs397516897

Orientation

minus

Stabilized

minus

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

Make rs397516897(-;-)

Make rs397516897(-;TGA)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140753334

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs397516897
dbSNP (classic)	rs397516897
ClinGen	rs397516897
ebi	rs397516897
HLI	rs397516897
Exac	rs397516897
Gnomad	rs397516897
Varsome	rs397516897
LitVar	rs397516897
Map	rs397516897
PheGenI	rs397516897
Biobank	rs397516897
1000 genomes	rs397516897
hgdp	rs397516897
ensembl	rs397516897
geneview	rs397516897
scholar	rs397516897
google	rs397516897
pharmgkb	rs397516897
gwascentral	rs397516897
openSNP	rs397516897
23andMe	rs397516897
SNPshot	rs397516897
SNPdbe	rs397516897
MSV3d	rs397516897
GWAS Ctlg	rs397516897

Max Magnitude

0

ClinVar
Risk	rs397516897(-;-)
Alt	rs397516897(-;-)
Reference	Rs397516897(TGA;TGA)
Significance	Probable-Pathogenic
Disease	Non-small cell lung cancer
Variation	info
Gene	BRAF
CLNDBN	Non-small cell lung cancer
Reversed	1
HGVS	NC_000007.13:g.140453134_140453136delTCA
CLNSRC	COSMIC
CLNACC	RCV000037937.2,