rs796065051

Orientation

minus

Stabilized

minus

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

Make rs796065051(C;T)

Make rs796065051(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

50319953

Gene

BRD7

is a	snp
is	mentioned by
dbSNP	rs796065051
dbSNP (classic)	rs796065051
ClinGen	rs796065051
ebi	rs796065051
HLI	rs796065051
Exac	rs796065051
Gnomad	rs796065051
Varsome	rs796065051
LitVar	rs796065051
Map	rs796065051
PheGenI	rs796065051
Biobank	rs796065051
1000 genomes	rs796065051
hgdp	rs796065051
ensembl	rs796065051
geneview	rs796065051
scholar	rs796065051
google	rs796065051
pharmgkb	rs796065051
gwascentral	rs796065051
openSNP	rs796065051
23andMe	rs796065051
SNPshot	rs796065051
SNPdbe	rs796065051
MSV3d	rs796065051
GWAS Ctlg	rs796065051

Max Magnitude

0

ClinVar
Risk	rs796065051(T;T)
Alt	rs796065051(T;T)
Reference	Rs796065051(C;C)
Significance	Probable-Pathogenic
Disease	malignant granular cell tumor
Variation	info
Gene	BRD7
CLNDBN	malignant granular cell tumor
Reversed	1
HGVS	NC_000016.9:g.50353864G>A
CLNSRC
CLNACC	RCV000190398.2,