rs876660385

Orientation

plus

Stabilized

plus

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

Make rs876660385(CAAT;CAAT)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32332338

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876660385
dbSNP (classic)	rs876660385
ClinGen	rs876660385
ebi	rs876660385
HLI	rs876660385
Exac	rs876660385
Gnomad	rs876660385
Varsome	rs876660385
LitVar	rs876660385
Map	rs876660385
PheGenI	rs876660385
Biobank	rs876660385
1000 genomes	rs876660385
hgdp	rs876660385
ensembl	rs876660385
geneview	rs876660385
scholar	rs876660385
google	rs876660385
pharmgkb	rs876660385
gwascentral	rs876660385
openSNP	rs876660385
23andMe	rs876660385
SNPshot	rs876660385
SNPdbe	rs876660385
MSV3d	rs876660385
GWAS Ctlg	rs876660385

Max Magnitude

6

ClinVar
Risk	rs876660385(TCAA;TCAA)
Alt	rs876660385(TCAA;TCAA)
Reference	Rs876660385(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32906472_32906475dupCAAT
CLNSRC
CLNACC	RCV000216716.1, RCV000257332.2,