rs397507625

Orientation

plus

Stabilized

plus

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

Make rs397507625(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336757

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507625
dbSNP (classic)	rs397507625
ClinGen	rs397507625
ebi	rs397507625
HLI	rs397507625
Exac	rs397507625
Gnomad	rs397507625
Varsome	rs397507625
LitVar	rs397507625
Map	rs397507625
PheGenI	rs397507625
Biobank	rs397507625
1000 genomes	rs397507625
hgdp	rs397507625
ensembl	rs397507625
geneview	rs397507625
scholar	rs397507625
google	rs397507625
pharmgkb	rs397507625
gwascentral	rs397507625
openSNP	rs397507625
23andMe	rs397507625
SNPshot	rs397507625
SNPdbe	rs397507625
MSV3d	rs397507625
GWAS Ctlg	rs397507625

Max Magnitude

6

ClinVar
Risk	rs397507625(-;-)
Alt	rs397507625(-;-)
Reference	Rs397507625(AACAATTATGA;AACAATTATGA)
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.32910894_32910904delACAATTATGAA
CLNSRC	ClinVar
CLNACC	RCV000043983.2, RCV000257653.2,