rs397507865

Orientation

plus

Stabilized

plus

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

Make rs397507865(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340886

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507865
dbSNP (classic)	rs397507865
ClinGen	rs397507865
ebi	rs397507865
HLI	rs397507865
Exac	rs397507865
Gnomad	rs397507865
Varsome	rs397507865
LitVar	rs397507865
Map	rs397507865
PheGenI	rs397507865
Biobank	rs397507865
1000 genomes	rs397507865
hgdp	rs397507865
ensembl	rs397507865
geneview	rs397507865
scholar	rs397507865
google	rs397507865
pharmgkb	rs397507865
gwascentral	rs397507865
openSNP	rs397507865
23andMe	rs397507865
SNPshot	rs397507865
SNPdbe	rs397507865
MSV3d	rs397507865
GWAS Ctlg	rs397507865

Max Magnitude

6

ClinVar
Risk	rs397507865(-;-)
Alt	rs397507865(-;-)
Reference	Rs397507865(CATT;CATT)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32915023_32915026delTCAT
CLNSRC	ClinVar
CLNACC	RCV000044977.4, RCV000221260.1, RCV000225746.2, RCV000241269.2,