rs878853304

Orientation

plus

Stabilized

plus

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

Make rs878853304(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32362657

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs878853304
dbSNP (classic)	rs878853304
ClinGen	rs878853304
ebi	rs878853304
HLI	rs878853304
Exac	rs878853304
Gnomad	rs878853304
Varsome	rs878853304
LitVar	rs878853304
Map	rs878853304
PheGenI	rs878853304
Biobank	rs878853304
1000 genomes	rs878853304
hgdp	rs878853304
ensembl	rs878853304
geneview	rs878853304
scholar	rs878853304
google	rs878853304
pharmgkb	rs878853304
gwascentral	rs878853304
openSNP	rs878853304
23andMe	rs878853304
SNPshot	rs878853304
SNPdbe	rs878853304
MSV3d	rs878853304
GWAS Ctlg	rs878853304

Max Magnitude

6

ClinVar
Risk	rs878853304(C;C)
Alt	rs878853304(C;C)
Reference	Rs878853304(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32936794_32936795insC
CLNSRC
CLNACC	RCV000225577.2,