rs397508015

Orientation

plus

Stabilized

plus

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

Make rs397508015(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379410

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508015
dbSNP (classic)	rs397508015
ClinGen	rs397508015
ebi	rs397508015
HLI	rs397508015
Exac	rs397508015
Gnomad	rs397508015
Varsome	rs397508015
LitVar	rs397508015
Map	rs397508015
PheGenI	rs397508015
Biobank	rs397508015
1000 genomes	rs397508015
hgdp	rs397508015
ensembl	rs397508015
geneview	rs397508015
scholar	rs397508015
google	rs397508015
pharmgkb	rs397508015
gwascentral	rs397508015
openSNP	rs397508015
23andMe	rs397508015
SNPshot	rs397508015
SNPdbe	rs397508015
MSV3d	rs397508015
GWAS Ctlg	rs397508015

Max Magnitude

6

ClinVar
Risk	rs397508015(-;-)
Alt	rs397508015(-;-)
Reference	Rs397508015(AGGA;AGGA)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32953547_32953550delAAGG
CLNSRC	ClinVar
CLNACC	RCV000045640.2, RCV000256756.2,