rs397507779

Orientation

plus

Stabilized

plus

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

Make rs397507779(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339705

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507779
dbSNP (classic)	rs397507779
ClinGen	rs397507779
ebi	rs397507779
HLI	rs397507779
Exac	rs397507779
Gnomad	rs397507779
Varsome	rs397507779
LitVar	rs397507779
Map	rs397507779
PheGenI	rs397507779
Biobank	rs397507779
1000 genomes	rs397507779
hgdp	rs397507779
ensembl	rs397507779
geneview	rs397507779
scholar	rs397507779
google	rs397507779
pharmgkb	rs397507779
gwascentral	rs397507779
openSNP	rs397507779
23andMe	rs397507779
SNPshot	rs397507779
SNPdbe	rs397507779
MSV3d	rs397507779
GWAS Ctlg	rs397507779

Max Magnitude

6

ClinVar
Risk	rs397507779(T;T)
Alt	rs397507779(T;T)
Reference	Rs397507779(AA;AA)
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.32913842_32913843delAAinsT
CLNSRC	ClinVar
CLNACC	RCV000044640.2, RCV000256629.2,