rs397507701

Orientation

plus

Stabilized

plus

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

Make rs397507701(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338360

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507701
dbSNP (classic)	rs397507701
ClinGen	rs397507701
ebi	rs397507701
HLI	rs397507701
Exac	rs397507701
Gnomad	rs397507701
Varsome	rs397507701
LitVar	rs397507701
Map	rs397507701
PheGenI	rs397507701
Biobank	rs397507701
1000 genomes	rs397507701
hgdp	rs397507701
ensembl	rs397507701
geneview	rs397507701
scholar	rs397507701
google	rs397507701
pharmgkb	rs397507701
gwascentral	rs397507701
openSNP	rs397507701
23andMe	rs397507701
SNPshot	rs397507701
SNPdbe	rs397507701
MSV3d	rs397507701
GWAS Ctlg	rs397507701

Max Magnitude

6

ClinVar
Risk	rs397507701(A;A)
Alt	rs397507701(A;A)
Reference	Rs397507701(-;-)
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.32912497dupA
CLNSRC	ClinVar
CLNACC	RCV000044331.2, RCV000256647.2,