rs397507767

Orientation

plus

Stabilized

plus

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

Make rs397507767(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339526

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507767
dbSNP (classic)	rs397507767
ClinGen	rs397507767
ebi	rs397507767
HLI	rs397507767
Exac	rs397507767
Gnomad	rs397507767
Varsome	rs397507767
LitVar	rs397507767
Map	rs397507767
PheGenI	rs397507767
Biobank	rs397507767
1000 genomes	rs397507767
hgdp	rs397507767
ensembl	rs397507767
geneview	rs397507767
scholar	rs397507767
google	rs397507767
pharmgkb	rs397507767
gwascentral	rs397507767
openSNP	rs397507767
23andMe	rs397507767
SNPshot	rs397507767
SNPdbe	rs397507767
MSV3d	rs397507767
GWAS Ctlg	rs397507767

Max Magnitude

6

aka c.5171delT

ClinVar
Risk	rs397507767(-;-)
Alt	rs397507767(-;-)
Reference	Rs397507767(T;T)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32913663delT
CLNSRC	ClinVar
CLNACC	RCV000044592.2,