rs121913377

Orientation

minus

Stabilized

minus

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

Make rs121913377(AT;AT)

Make rs121913377(AT;TG)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

140753335

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913377
dbSNP (classic)	rs121913377
ClinGen	rs121913377
ebi	rs121913377
HLI	rs121913377
Exac	rs121913377
Gnomad	rs121913377
Varsome	rs121913377
LitVar	rs121913377
Map	rs121913377
PheGenI	rs121913377
Biobank	rs121913377
1000 genomes	rs121913377
hgdp	rs121913377
ensembl	rs121913377
geneview	rs121913377
scholar	rs121913377
google	rs121913377
pharmgkb	rs121913377
gwascentral	rs121913377
openSNP	rs121913377
23andMe	rs121913377
SNPshot	rs121913377
SNPdbe	rs121913377
MSV3d	rs121913377
GWAS Ctlg	rs121913377

Max Magnitude

0

ClinVar
Risk	rs121913377(AA;AA) rs121913377(AT;AT)
Alt	rs121913377(AA;AA) rs121913377(AT;AT)
Reference	Rs121913377(TG;TG)
Significance	Pathogenic
Disease	Malignant melanoma Colonic Neoplasms
Variation	info
Gene	BRAF
CLNDBN	Malignant melanoma Colonic Neoplasms
Reversed	1
HGVS	NC_000007.13:g.140453135_140453136delCAinsAT; NC_000007.13:g.140453135_140453136delCAinsTT
CLNSRC
CLNACC	RCV000423512.1, RCV000424781.1, RCV000442563.1,