rs397507788

Orientation

plus

Stabilized

plus

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

Make rs397507788(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339924

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507788
dbSNP (classic)	rs397507788
ClinGen	rs397507788
ebi	rs397507788
HLI	rs397507788
Exac	rs397507788
Gnomad	rs397507788
Varsome	rs397507788
LitVar	rs397507788
Map	rs397507788
PheGenI	rs397507788
Biobank	rs397507788
1000 genomes	rs397507788
hgdp	rs397507788
ensembl	rs397507788
geneview	rs397507788
scholar	rs397507788
google	rs397507788
pharmgkb	rs397507788
gwascentral	rs397507788
openSNP	rs397507788
23andMe	rs397507788
SNPshot	rs397507788
SNPdbe	rs397507788
MSV3d	rs397507788
GWAS Ctlg	rs397507788

Max Magnitude

6

aka c.5569_5573delGAAAC (p.Glu1857Asnfs)

23andMe name: i5009097

ClinVar
Risk	rs397507788(-;-)
Alt	rs397507788(-;-)
Reference	Rs397507788(GAAAC;GAAAC)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32914061_32914065delGAAAC
CLNSRC	ClinVar
CLNACC	RCV000044683.2, RCV000167362.1, RCV000168578.4, RCV000257914.1,