rs397507778

Orientation

plus

Stabilized

plus

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

Make rs397507778(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339646

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507778
dbSNP (classic)	rs397507778
ClinGen	rs397507778
ebi	rs397507778
HLI	rs397507778
Exac	rs397507778
Gnomad	rs397507778
Varsome	rs397507778
LitVar	rs397507778
Map	rs397507778
PheGenI	rs397507778
Biobank	rs397507778
1000 genomes	rs397507778
hgdp	rs397507778
ensembl	rs397507778
geneview	rs397507778
scholar	rs397507778
google	rs397507778
pharmgkb	rs397507778
gwascentral	rs397507778
openSNP	rs397507778
23andMe	rs397507778
SNPshot	rs397507778
SNPdbe	rs397507778
MSV3d	rs397507778
GWAS Ctlg	rs397507778

Max Magnitude

6

ClinVar
Risk	rs397507778(G;G)
Alt	rs397507778(G;G)
Reference	Rs397507778(C;C)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32913783C>G
CLNSRC	ClinVar
CLNACC	RCV000044630.2,