rs397507780

Orientation

plus

Stabilized

plus

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

Make rs397507780(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339708

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507780
dbSNP (classic)	rs397507780
ClinGen	rs397507780
ebi	rs397507780
HLI	rs397507780
Exac	rs397507780
Gnomad	rs397507780
Varsome	rs397507780
LitVar	rs397507780
Map	rs397507780
PheGenI	rs397507780
Biobank	rs397507780
1000 genomes	rs397507780
hgdp	rs397507780
ensembl	rs397507780
geneview	rs397507780
scholar	rs397507780
google	rs397507780
pharmgkb	rs397507780
gwascentral	rs397507780
openSNP	rs397507780
23andMe	rs397507780
SNPshot	rs397507780
SNPdbe	rs397507780
MSV3d	rs397507780
GWAS Ctlg	rs397507780

Max Magnitude

6

ClinVar
Risk	rs397507780(-;-)
Alt	rs397507780(-;-)
Reference	Rs397507780(AC;AC)
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.32913845_32913846delAC
CLNSRC	ClinVar
CLNACC	RCV000044643.2, RCV000257574.2,