rs397507618

Orientation

plus

Stabilized

plus

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

Make rs397507618(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336505

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507618
dbSNP (classic)	rs397507618
ClinGen	rs397507618
ebi	rs397507618
HLI	rs397507618
Exac	rs397507618
Gnomad	rs397507618
Varsome	rs397507618
LitVar	rs397507618
Map	rs397507618
PheGenI	rs397507618
Biobank	rs397507618
1000 genomes	rs397507618
hgdp	rs397507618
ensembl	rs397507618
geneview	rs397507618
scholar	rs397507618
google	rs397507618
pharmgkb	rs397507618
gwascentral	rs397507618
openSNP	rs397507618
23andMe	rs397507618
SNPshot	rs397507618
SNPdbe	rs397507618
MSV3d	rs397507618
GWAS Ctlg	rs397507618

Max Magnitude

6

ClinVar
Risk	rs397507618(-;-)
Alt	rs397507618(-;-)
Reference	Rs397507618(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32910642delG
CLNSRC	ClinVar
CLNACC	RCV000043951.2, RCV000241041.2, RCV000482272.1,