rs876660755

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;A)	6	BRCA2 variant considered pathogenic for breast cancer
(A;A)	0	common in clinvar

Make rs876660755(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32338802

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876660755
dbSNP (classic)	rs876660755
ClinGen	rs876660755
ebi	rs876660755
HLI	rs876660755
Exac	rs876660755
Gnomad	rs876660755
Varsome	rs876660755
LitVar	rs876660755
Map	rs876660755
PheGenI	rs876660755
Biobank	rs876660755
1000 genomes	rs876660755
hgdp	rs876660755
ensembl	rs876660755
geneview	rs876660755
scholar	rs876660755
google	rs876660755
pharmgkb	rs876660755
gwascentral	rs876660755
openSNP	rs876660755
23andMe	rs876660755
SNPshot	rs876660755
SNPdbe	rs876660755
MSV3d	rs876660755
GWAS Ctlg	rs876660755

Max Magnitude

6

aka c.4447delA

ClinVar
Risk	rs876660755(-;-)
Alt	rs876660755(-;-)
Reference	Rs876660755(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32912939delA
CLNSRC
CLNACC	RCV000218196.1,