rs397507695

Orientation

plus

Stabilized

plus

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

Make rs397507695(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338242

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507695
ClinGen	rs397507695
ebi	rs397507695
HLI	rs397507695
Exac	rs397507695
Varsome	rs397507695
Map	rs397507695
PheGenI	rs397507695
hapmap	rs397507695
1000 genomes	rs397507695
hgdp	rs397507695
ensembl	rs397507695
gopubmed	rs397507695
geneview	rs397507695
scholar	rs397507695
google	rs397507695
pharmgkb	rs397507695
gwascentral	rs397507695
openSNP	rs397507695
23andMe	rs397507695
23andMe all	rs397507695
SNP Nexus
SNPshot	rs397507695
SNPdbe	rs397507695
MSV3d	rs397507695
GWAS Ctlg	rs397507695

Max Magnitude

6

ClinVar
Risk	rs397507695(-;-)
Alt	rs397507695(-;-)
Reference	Rs397507695(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32912379delA
CLNSRC	ClinVar
CLNACC	RCV000044297.2, RCV000256738.1, RCV000257940.1,