rs587782378

Orientation

plus

Stabilized

plus

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

Make rs587782378(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32380083

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587782378
dbSNP (classic)	rs587782378
ClinGen	rs587782378
ebi	rs587782378
HLI	rs587782378
Exac	rs587782378
Gnomad	rs587782378
Varsome	rs587782378
LitVar	rs587782378
Map	rs587782378
PheGenI	rs587782378
Biobank	rs587782378
1000 genomes	rs587782378
hgdp	rs587782378
ensembl	rs587782378
geneview	rs587782378
scholar	rs587782378
google	rs587782378
pharmgkb	rs587782378
gwascentral	rs587782378
openSNP	rs587782378
23andMe	rs587782378
SNPshot	rs587782378
SNPdbe	rs587782378
MSV3d	rs587782378
GWAS Ctlg	rs587782378

Max Magnitude

6

aka c.9194_9195delTT

ClinVar
Risk	rs587782378(-;-)
Alt	rs587782378(-;-)
Reference	Rs587782378(TT;TT)
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.32954220_32954221delTT
CLNSRC
CLNACC	RCV000131371.2, RCV000241374.1,