rs397507616

Orientation

plus

Stabilized

plus

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

Make rs397507616(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336288

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507616
dbSNP (classic)	rs397507616
ClinGen	rs397507616
ebi	rs397507616
HLI	rs397507616
Exac	rs397507616
Gnomad	rs397507616
Varsome	rs397507616
LitVar	rs397507616
Map	rs397507616
PheGenI	rs397507616
Biobank	rs397507616
1000 genomes	rs397507616
hgdp	rs397507616
ensembl	rs397507616
geneview	rs397507616
scholar	rs397507616
google	rs397507616
pharmgkb	rs397507616
gwascentral	rs397507616
openSNP	rs397507616
23andMe	rs397507616
SNPshot	rs397507616
SNPdbe	rs397507616
MSV3d	rs397507616
GWAS Ctlg	rs397507616

Max Magnitude

6

ClinVar
Risk	rs397507616(-;-)
Alt	rs397507616(-;-)
Reference	Rs397507616(A;A)
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.32910425delA
CLNSRC	ClinVar
CLNACC	RCV000043927.2, RCV000256978.1,