rs587781804

Orientation

plus

Stabilized

plus

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

Make rs587781804(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32332906

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587781804
dbSNP (classic)	rs587781804
ClinGen	rs587781804
ebi	rs587781804
HLI	rs587781804
Exac	rs587781804
Gnomad	rs587781804
Varsome	rs587781804
LitVar	rs587781804
Map	rs587781804
PheGenI	rs587781804
Biobank	rs587781804
1000 genomes	rs587781804
hgdp	rs587781804
ensembl	rs587781804
geneview	rs587781804
scholar	rs587781804
google	rs587781804
pharmgkb	rs587781804
gwascentral	rs587781804
openSNP	rs587781804
23andMe	rs587781804
SNPshot	rs587781804
SNPdbe	rs587781804
MSV3d	rs587781804
GWAS Ctlg	rs587781804

Max Magnitude

6

ClinVar
Risk	rs587781804(-;-)
Alt	rs587781804(-;-)
Reference	Rs587781804(TCAT;TCAT)
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.32907043_32907046delTCAT
CLNSRC
CLNACC	RCV000130073.2, RCV000241413.1,