rs876659767

Orientation

plus

Stabilized

plus

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

Make rs876659767(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32337071

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876659767
dbSNP (classic)	rs876659767
ClinGen	rs876659767
ebi	rs876659767
HLI	rs876659767
Exac	rs876659767
Gnomad	rs876659767
Varsome	rs876659767
LitVar	rs876659767
Map	rs876659767
PheGenI	rs876659767
Biobank	rs876659767
1000 genomes	rs876659767
hgdp	rs876659767
ensembl	rs876659767
geneview	rs876659767
scholar	rs876659767
google	rs876659767
pharmgkb	rs876659767
gwascentral	rs876659767
openSNP	rs876659767
23andMe	rs876659767
SNPshot	rs876659767
SNPdbe	rs876659767
MSV3d	rs876659767
GWAS Ctlg	rs876659767

Max Magnitude

6

aka c.2716dupA (p.Thr906fs)

ClinVar
Risk	rs876659767(A;A)
Alt	rs876659767(A;A)
Reference	Rs876659767(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32911208dupA
CLNSRC
CLNACC	RCV000221474.1,