rs397507956

Orientation

plus

Stabilized

plus

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

Make rs397507956(AG;AG)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363235

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507956
dbSNP (classic)	rs397507956
ClinGen	rs397507956
ebi	rs397507956
HLI	rs397507956
Exac	rs397507956
Gnomad	rs397507956
Varsome	rs397507956
LitVar	rs397507956
Map	rs397507956
PheGenI	rs397507956
Biobank	rs397507956
1000 genomes	rs397507956
hgdp	rs397507956
ensembl	rs397507956
geneview	rs397507956
scholar	rs397507956
google	rs397507956
pharmgkb	rs397507956
gwascentral	rs397507956
openSNP	rs397507956
23andMe	rs397507956
SNPshot	rs397507956
SNPdbe	rs397507956
MSV3d	rs397507956
GWAS Ctlg	rs397507956

Max Magnitude

6

ClinVar
Risk	rs397507956(AG;AG)
Alt	rs397507956(AG;AG)
Reference	Rs397507956(-;-)
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.32937371_32937372dupAG
CLNSRC	ClinVar
CLNACC	RCV000045395.2, RCV000257724.2,