rs397507577

Orientation

plus

Stabilized

plus

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

Make rs397507577(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332778

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507577
ClinGen	rs397507577
ebi	rs397507577
HLI	rs397507577
Exac	rs397507577
Varsome	rs397507577
Map	rs397507577
PheGenI	rs397507577
hapmap	rs397507577
1000 genomes	rs397507577
hgdp	rs397507577
ensembl	rs397507577
gopubmed	rs397507577
geneview	rs397507577
scholar	rs397507577
google	rs397507577
pharmgkb	rs397507577
gwascentral	rs397507577
openSNP	rs397507577
23andMe	rs397507577
23andMe all	rs397507577
SNP Nexus
SNPshot	rs397507577
SNPdbe	rs397507577
MSV3d	rs397507577
GWAS Ctlg	rs397507577

Max Magnitude

6

ClinVar
Risk	rs397507577(-;-)
Alt	rs397507577(-;-)
Reference	Rs397507577(AAAA;AAAA)
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.32906915_32906918delAAAA
CLNSRC	ClinVar
CLNACC	RCV000043776.2, RCV000257480.2,