rs397507598

Orientation

plus

Stabilized

plus

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

Make rs397507598(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32333114

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507598
dbSNP (classic)	rs397507598
ClinGen	rs397507598
ebi	rs397507598
HLI	rs397507598
Exac	rs397507598
Gnomad	rs397507598
Varsome	rs397507598
LitVar	rs397507598
Map	rs397507598
PheGenI	rs397507598
Biobank	rs397507598
1000 genomes	rs397507598
hgdp	rs397507598
ensembl	rs397507598
geneview	rs397507598
scholar	rs397507598
google	rs397507598
pharmgkb	rs397507598
gwascentral	rs397507598
openSNP	rs397507598
23andMe	rs397507598
SNPshot	rs397507598
SNPdbe	rs397507598
MSV3d	rs397507598
GWAS Ctlg	rs397507598

Max Magnitude

6

ClinVar
Risk	rs397507598(-;-)
Alt	rs397507598(-;-)
Reference	Rs397507598(T;T)
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.32907251delT
CLNSRC	ClinVar
CLNACC	RCV000043849.2, RCV000241220.2,