rs397507578

Orientation

plus

Stabilized

plus

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

Make rs397507578(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332788

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507578
dbSNP (classic)	rs397507578
ClinGen	rs397507578
ebi	rs397507578
HLI	rs397507578
Exac	rs397507578
Gnomad	rs397507578
Varsome	rs397507578
LitVar	rs397507578
Map	rs397507578
PheGenI	rs397507578
Biobank	rs397507578
1000 genomes	rs397507578
hgdp	rs397507578
ensembl	rs397507578
geneview	rs397507578
scholar	rs397507578
google	rs397507578
pharmgkb	rs397507578
gwascentral	rs397507578
openSNP	rs397507578
23andMe	rs397507578
SNPshot	rs397507578
SNPdbe	rs397507578
MSV3d	rs397507578
GWAS Ctlg	rs397507578

Max Magnitude

6

aka c.1310_1311delAA (p.Lys437fs)

ClinVar
Risk	rs397507578(-;-)
Alt	rs397507578(-;-)
Reference	Rs397507578(AA;AA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32906925_32906926delAA
CLNSRC	ClinVar
CLNACC	RCV000043778.2,