rs397507575

Orientation

plus

Stabilized

plus

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

Make rs397507575(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332658

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507575
dbSNP (classic)	rs397507575
ClinGen	rs397507575
ebi	rs397507575
HLI	rs397507575
Exac	rs397507575
Gnomad	rs397507575
Varsome	rs397507575
LitVar	rs397507575
Map	rs397507575
PheGenI	rs397507575
Biobank	rs397507575
1000 genomes	rs397507575
hgdp	rs397507575
ensembl	rs397507575
geneview	rs397507575
scholar	rs397507575
google	rs397507575
pharmgkb	rs397507575
gwascentral	rs397507575
openSNP	rs397507575
23andMe	rs397507575
SNPshot	rs397507575
SNPdbe	rs397507575
MSV3d	rs397507575
GWAS Ctlg	rs397507575

Max Magnitude

6

ClinVar
Risk	rs397507575(T;T)
Alt	rs397507575(T;T)
Reference	Rs397507575(G;G)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32906795G>T
CLNSRC	ClinVar
CLNACC	RCV000043751.2,