rs397507807

Orientation

plus

Stabilized

plus

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

Make rs397507807(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340154

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507807
dbSNP (classic)	rs397507807
ClinGen	rs397507807
ebi	rs397507807
HLI	rs397507807
Exac	rs397507807
Gnomad	rs397507807
Varsome	rs397507807
LitVar	rs397507807
Map	rs397507807
PheGenI	rs397507807
Biobank	rs397507807
1000 genomes	rs397507807
hgdp	rs397507807
ensembl	rs397507807
geneview	rs397507807
scholar	rs397507807
google	rs397507807
pharmgkb	rs397507807
gwascentral	rs397507807
openSNP	rs397507807
23andMe	rs397507807
SNPshot	rs397507807
SNPdbe	rs397507807
MSV3d	rs397507807
GWAS Ctlg	rs397507807

Max Magnitude

6

aka c.5799_5800delCC

ClinVar
Risk	rs397507807(-;-)
Alt	rs397507807(-;-)
Reference	Rs397507807(CC;CC)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32914291_32914292delCC
CLNSRC	ClinVar
CLNACC	RCV000044760.2,