rs397507717

Orientation

plus

Stabilized

plus

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

Make rs397507717(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326114

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507717
dbSNP (classic)	rs397507717
ClinGen	rs397507717
ebi	rs397507717
HLI	rs397507717
Exac	rs397507717
Gnomad	rs397507717
Varsome	rs397507717
LitVar	rs397507717
Map	rs397507717
PheGenI	rs397507717
Biobank	rs397507717
1000 genomes	rs397507717
hgdp	rs397507717
ensembl	rs397507717
geneview	rs397507717
scholar	rs397507717
google	rs397507717
pharmgkb	rs397507717
gwascentral	rs397507717
openSNP	rs397507717
23andMe	rs397507717
SNPshot	rs397507717
SNPdbe	rs397507717
MSV3d	rs397507717
GWAS Ctlg	rs397507717

Max Magnitude

6

ClinVar
Risk	rs397507717(T;T)
Alt	rs397507717(T;T)
Reference	Rs397507717(C;C)
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.32900251C>T
CLNSRC	ClinVar
CLNACC	RCV000044405.2, RCV000241305.2,