rs397507968

Orientation

plus

Stabilized

plus

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

Make rs397507968(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363408

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507968
dbSNP (classic)	rs397507968
ClinGen	rs397507968
ebi	rs397507968
HLI	rs397507968
Exac	rs397507968
Gnomad	rs397507968
Varsome	rs397507968
LitVar	rs397507968
Map	rs397507968
PheGenI	rs397507968
Biobank	rs397507968
1000 genomes	rs397507968
hgdp	rs397507968
ensembl	rs397507968
geneview	rs397507968
scholar	rs397507968
google	rs397507968
pharmgkb	rs397507968
gwascentral	rs397507968
openSNP	rs397507968
23andMe	rs397507968
SNPshot	rs397507968
SNPdbe	rs397507968
MSV3d	rs397507968
GWAS Ctlg	rs397507968

Merged from

Rs757730855

Max Magnitude

6

ClinVar
Risk	rs397507968(C;C)
Alt	rs397507968(C;C)
Reference	Rs397507968(-;-)
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.32937545dupC
CLNSRC	ClinVar
CLNACC	RCV000045451.2, RCV000241496.2,