rs876659278

Orientation

plus

Stabilized

plus

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

Make rs876659278(-;-)

Make rs876659278(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32333167

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876659278
dbSNP (classic)	rs876659278
ClinGen	rs876659278
ebi	rs876659278
HLI	rs876659278
Exac	rs876659278
Gnomad	rs876659278
Varsome	rs876659278
LitVar	rs876659278
Map	rs876659278
PheGenI	rs876659278
Biobank	rs876659278
1000 genomes	rs876659278
hgdp	rs876659278
ensembl	rs876659278
geneview	rs876659278
scholar	rs876659278
google	rs876659278
pharmgkb	rs876659278
gwascentral	rs876659278
openSNP	rs876659278
23andMe	rs876659278
SNPshot	rs876659278
SNPdbe	rs876659278
MSV3d	rs876659278
GWAS Ctlg	rs876659278

Max Magnitude

0

ClinVar
Risk	rs876659278(-;-)
Alt	rs876659278(-;-)
Reference	Rs876659278(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32907304delG
CLNSRC
CLNACC	RCV000213086.1,