rs587782075

Orientation

plus

Stabilized

plus

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

Make rs587782075(TA;TA)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32339527

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587782075
dbSNP (classic)	rs587782075
ClinGen	rs587782075
ebi	rs587782075
HLI	rs587782075
Exac	rs587782075
Gnomad	rs587782075
Varsome	rs587782075
LitVar	rs587782075
Map	rs587782075
PheGenI	rs587782075
Biobank	rs587782075
1000 genomes	rs587782075
hgdp	rs587782075
ensembl	rs587782075
geneview	rs587782075
scholar	rs587782075
google	rs587782075
pharmgkb	rs587782075
gwascentral	rs587782075
openSNP	rs587782075
23andMe	rs587782075
SNPshot	rs587782075
SNPdbe	rs587782075
MSV3d	rs587782075
GWAS Ctlg	rs587782075

Max Magnitude

6

ClinVar
Risk	rs587782075(TA;TA)
Alt	rs587782075(TA;TA)
Reference	Rs587782075(-;-)
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.32913663_32913664dupTA
CLNSRC
CLNACC	RCV000130567.2, RCV000211017.2,