rs397507817

Orientation

plus

Stabilized

plus

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

Make rs397507817(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340319

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507817
dbSNP (classic)	rs397507817
ClinGen	rs397507817
ebi	rs397507817
HLI	rs397507817
Exac	rs397507817
Gnomad	rs397507817
Varsome	rs397507817
LitVar	rs397507817
Map	rs397507817
PheGenI	rs397507817
Biobank	rs397507817
1000 genomes	rs397507817
hgdp	rs397507817
ensembl	rs397507817
geneview	rs397507817
scholar	rs397507817
google	rs397507817
pharmgkb	rs397507817
gwascentral	rs397507817
openSNP	rs397507817
23andMe	rs397507817
SNPshot	rs397507817
SNPdbe	rs397507817
MSV3d	rs397507817
GWAS Ctlg	rs397507817

Max Magnitude

6

aka c.5964_5965delAT

ClinVar
Risk	rs397507817(-;-)
Alt	rs397507817(-;-)
Reference	Rs397507817(TA;TA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32914456_32914457delAT
CLNSRC	ClinVar
CLNACC	RCV000044805.2,