rs886040446

Orientation

plus

Stabilized

plus

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

Make rs886040446(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32337119

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886040446
dbSNP (classic)	rs886040446
ClinGen	rs886040446
ebi	rs886040446
HLI	rs886040446
Exac	rs886040446
Gnomad	rs886040446
Varsome	rs886040446
LitVar	rs886040446
Map	rs886040446
PheGenI	rs886040446
Biobank	rs886040446
1000 genomes	rs886040446
hgdp	rs886040446
ensembl	rs886040446
geneview	rs886040446
scholar	rs886040446
google	rs886040446
pharmgkb	rs886040446
gwascentral	rs886040446
openSNP	rs886040446
23andMe	rs886040446
SNPshot	rs886040446
SNPdbe	rs886040446
MSV3d	rs886040446
GWAS Ctlg	rs886040446

Max Magnitude

6

ClinVar
Risk	rs886040446(-;-)
Alt	rs886040446(-;-)
Reference	Rs886040446(TTCAAGAACTCTAC;TTCAAGAACTCTAC)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911256_32911269delTTCAAGAACTCTAC
CLNSRC
CLNACC	RCV000257441.2,