rs397507406

Orientation

plus

Stabilized

plus

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

Make rs397507406(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32371016

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507406
dbSNP (classic)	rs397507406
ClinGen	rs397507406
ebi	rs397507406
HLI	rs397507406
Exac	rs397507406
Gnomad	rs397507406
Varsome	rs397507406
LitVar	rs397507406
Map	rs397507406
PheGenI	rs397507406
Biobank	rs397507406
1000 genomes	rs397507406
hgdp	rs397507406
ensembl	rs397507406
geneview	rs397507406
scholar	rs397507406
google	rs397507406
pharmgkb	rs397507406
gwascentral	rs397507406
openSNP	rs397507406
23andMe	rs397507406
SNPshot	rs397507406
SNPdbe	rs397507406
MSV3d	rs397507406
GWAS Ctlg	rs397507406

Max Magnitude

6

ClinVar
Risk	rs397507406(-;-)
Alt	rs397507406(-;-)
Reference	Rs397507406(AAGG;AAGG)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast not provided
Reversed	0
HGVS	NC_000013.10:g.32945153_32945156delGAAG
CLNSRC	ClinVar
CLNACC	RCV000031750.4, RCV000045555.2, RCV000484733.1,