rs397507642

Orientation

plus

Stabilized

plus

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

Make rs397507642(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337141

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507642
ClinGen	rs397507642
ebi	rs397507642
HLI	rs397507642
Exac	rs397507642
Varsome	rs397507642
Map	rs397507642
PheGenI	rs397507642
hapmap	rs397507642
1000 genomes	rs397507642
hgdp	rs397507642
ensembl	rs397507642
gopubmed	rs397507642
geneview	rs397507642
scholar	rs397507642
google	rs397507642
pharmgkb	rs397507642
gwascentral	rs397507642
openSNP	rs397507642
23andMe	rs397507642
23andMe all	rs397507642
SNP Nexus
SNPshot	rs397507642
SNPdbe	rs397507642
MSV3d	rs397507642
GWAS Ctlg	rs397507642

Max Magnitude

6

ClinVar
Risk	rs397507642(-;-)
Alt	rs397507642(-;-)
Reference	Rs397507642(T;T)
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.32911278delT
CLNSRC	ClinVar
CLNACC	RCV000044056.2, RCV000256522.2,