rs397507705

Orientation

plus

Stabilized

plus

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

Make rs397507705(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338456

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507705
dbSNP (classic)	rs397507705
ClinGen	rs397507705
ebi	rs397507705
HLI	rs397507705
Exac	rs397507705
Gnomad	rs397507705
Varsome	rs397507705
LitVar	rs397507705
Map	rs397507705
PheGenI	rs397507705
Biobank	rs397507705
1000 genomes	rs397507705
hgdp	rs397507705
ensembl	rs397507705
geneview	rs397507705
scholar	rs397507705
google	rs397507705
pharmgkb	rs397507705
gwascentral	rs397507705
openSNP	rs397507705
23andMe	rs397507705
SNPshot	rs397507705
SNPdbe	rs397507705
MSV3d	rs397507705
GWAS Ctlg	rs397507705

Max Magnitude

6

aka c.4101dupA and also c.4101delA, both of which are considered pathogenic for breast cancer in ClinVar

ClinVar
Risk	rs397507705(-;-)
Alt	rs397507705(-;-)
Reference	Rs397507705(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912593delA
CLNSRC	ClinVar
CLNACC	RCV000044350.2, RCV000256668.2,