rs397507751

Orientation

plus

Stabilized

plus

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

Make rs397507751(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339295

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507751
dbSNP (classic)	rs397507751
ClinGen	rs397507751
ebi	rs397507751
HLI	rs397507751
Exac	rs397507751
Gnomad	rs397507751
Varsome	rs397507751
LitVar	rs397507751
Map	rs397507751
PheGenI	rs397507751
Biobank	rs397507751
1000 genomes	rs397507751
hgdp	rs397507751
ensembl	rs397507751
geneview	rs397507751
scholar	rs397507751
google	rs397507751
pharmgkb	rs397507751
gwascentral	rs397507751
openSNP	rs397507751
23andMe	rs397507751
SNPshot	rs397507751
SNPdbe	rs397507751
MSV3d	rs397507751
GWAS Ctlg	rs397507751

Max Magnitude

6

ClinVar
Risk	rs397507751(-;-)
Alt	rs397507751(-;-)
Reference	Rs397507751(AC;AC)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32913432_32913433delCA
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000044528.2, RCV000077342.4, RCV000132504.3, RCV000487067.1,