rs397507673

Orientation

plus

Stabilized

plus

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

Make rs397507673(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337886

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507673
dbSNP (classic)	rs397507673
ClinGen	rs397507673
ebi	rs397507673
HLI	rs397507673
Exac	rs397507673
Gnomad	rs397507673
Varsome	rs397507673
LitVar	rs397507673
Map	rs397507673
PheGenI	rs397507673
Biobank	rs397507673
1000 genomes	rs397507673
hgdp	rs397507673
ensembl	rs397507673
geneview	rs397507673
scholar	rs397507673
google	rs397507673
pharmgkb	rs397507673
gwascentral	rs397507673
openSNP	rs397507673
23andMe	rs397507673
SNPshot	rs397507673
SNPdbe	rs397507673
MSV3d	rs397507673
GWAS Ctlg	rs397507673

Max Magnitude

6

aka c.3531_3534delCAGC (p.Asp1177Glufs)

23andMe name: i5009174

ClinVar
Risk	rs397507673(-;-)
Alt	rs397507673(-;-)
Reference	Rs397507673(CAGC;CAGC)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32912023_32912026delCAGC
CLNSRC	ClinVar
CLNACC	RCV000044215.2,