rs397507987

Orientation

plus

Stabilized

plus

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

Make rs397507987(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32370521

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507987
dbSNP (classic)	rs397507987
ClinGen	rs397507987
ebi	rs397507987
HLI	rs397507987
Exac	rs397507987
Gnomad	rs397507987
Varsome	rs397507987
LitVar	rs397507987
Map	rs397507987
PheGenI	rs397507987
Biobank	rs397507987
1000 genomes	rs397507987
hgdp	rs397507987
ensembl	rs397507987
geneview	rs397507987
scholar	rs397507987
google	rs397507987
pharmgkb	rs397507987
gwascentral	rs397507987
openSNP	rs397507987
23andMe	rs397507987
SNPshot	rs397507987
SNPdbe	rs397507987
MSV3d	rs397507987
GWAS Ctlg	rs397507987

Max Magnitude

6

ClinVar
Risk	rs397507987(A;A)
Alt	rs397507987(A;A)
Reference	Rs397507987(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.32944658T>A
CLNSRC	ClinVar
CLNACC	RCV000045522.2, RCV000256626.2,