rs397507850

Orientation

plus

Stabilized

plus

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

Make rs397507850(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340761

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507850
dbSNP (classic)	rs397507850
ClinGen	rs397507850
ebi	rs397507850
HLI	rs397507850
Exac	rs397507850
Gnomad	rs397507850
Varsome	rs397507850
LitVar	rs397507850
Map	rs397507850
PheGenI	rs397507850
Biobank	rs397507850
1000 genomes	rs397507850
hgdp	rs397507850
ensembl	rs397507850
geneview	rs397507850
scholar	rs397507850
google	rs397507850
pharmgkb	rs397507850
gwascentral	rs397507850
openSNP	rs397507850
23andMe	rs397507850
SNPshot	rs397507850
SNPdbe	rs397507850
MSV3d	rs397507850
GWAS Ctlg	rs397507850

Max Magnitude

6

aka c.6406_6407delTT

ClinVar
Risk	rs397507850(-;-)
Alt	rs397507850(-;-)
Reference	Rs397507850(TT;TT)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32914898_32914899delTT
CLNSRC	ClinVar
CLNACC	RCV000044935.2,