rs397507640

Orientation

plus

Stabilized

plus

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

Make rs397507640(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337128

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507640
dbSNP (classic)	rs397507640
ClinGen	rs397507640
ebi	rs397507640
HLI	rs397507640
Exac	rs397507640
Gnomad	rs397507640
Varsome	rs397507640
LitVar	rs397507640
Map	rs397507640
PheGenI	rs397507640
Biobank	rs397507640
1000 genomes	rs397507640
hgdp	rs397507640
ensembl	rs397507640
geneview	rs397507640
scholar	rs397507640
google	rs397507640
pharmgkb	rs397507640
gwascentral	rs397507640
openSNP	rs397507640
23andMe	rs397507640
SNPshot	rs397507640
SNPdbe	rs397507640
MSV3d	rs397507640
GWAS Ctlg	rs397507640

Max Magnitude

6

aka c.2773dupT (p.Ser925fs)

ClinVar
Risk	rs397507640(T;T)
Alt	rs397507640(T;T)
Reference	Rs397507640(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32911265dupT
CLNSRC	ClinVar
CLNACC	RCV000044053.2,