rs397507814

Orientation

plus

Stabilized

plus

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

Make rs397507814(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340307

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507814
dbSNP (classic)	rs397507814
ClinGen	rs397507814
ebi	rs397507814
HLI	rs397507814
Exac	rs397507814
Gnomad	rs397507814
Varsome	rs397507814
LitVar	rs397507814
Map	rs397507814
PheGenI	rs397507814
Biobank	rs397507814
1000 genomes	rs397507814
hgdp	rs397507814
ensembl	rs397507814
geneview	rs397507814
scholar	rs397507814
google	rs397507814
pharmgkb	rs397507814
gwascentral	rs397507814
openSNP	rs397507814
23andMe	rs397507814
SNPshot	rs397507814
SNPdbe	rs397507814
MSV3d	rs397507814
GWAS Ctlg	rs397507814

Max Magnitude

6

ClinVar
Risk	rs397507814(A;A)
Alt	rs397507814(A;A)
Reference	Rs397507814(-;-)
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.32914444dupA
CLNSRC	ClinVar
CLNACC	RCV000044801.2, RCV000162056.2,