rs397507840

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs397507840(A;G)

Make rs397507840(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326616

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507840
dbSNP (classic)	rs397507840
ClinGen	rs397507840
ebi	rs397507840
HLI	rs397507840
Exac	rs397507840
Gnomad	rs397507840
Varsome	rs397507840
LitVar	rs397507840
Map	rs397507840
PheGenI	rs397507840
Biobank	rs397507840
1000 genomes	rs397507840
hgdp	rs397507840
ensembl	rs397507840
geneview	rs397507840
scholar	rs397507840
google	rs397507840
pharmgkb	rs397507840
gwascentral	rs397507840
openSNP	rs397507840
23andMe	rs397507840
SNPshot	rs397507840
SNPdbe	rs397507840
MSV3d	rs397507840
GWAS Ctlg	rs397507840

Max Magnitude

0

ClinVar
Risk	rs397507840(G;G)
Alt	rs397507840(G;G)
Reference	Rs397507840(A;A)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32900753A>G
CLNSRC	ClinVar
CLNACC	RCV000044898.3, RCV000258233.1,