rs397507872

Orientation

plus

Stabilized

plus

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

Make rs397507872(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340990

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507872
dbSNP (classic)	rs397507872
ClinGen	rs397507872
ebi	rs397507872
HLI	rs397507872
Exac	rs397507872
Gnomad	rs397507872
Varsome	rs397507872
LitVar	rs397507872
Map	rs397507872
PheGenI	rs397507872
Biobank	rs397507872
1000 genomes	rs397507872
hgdp	rs397507872
ensembl	rs397507872
geneview	rs397507872
scholar	rs397507872
google	rs397507872
pharmgkb	rs397507872
gwascentral	rs397507872
openSNP	rs397507872
23andMe	rs397507872
SNPshot	rs397507872
SNPdbe	rs397507872
MSV3d	rs397507872
GWAS Ctlg	rs397507872

Max Magnitude

6

c.6635_6636delGT

ClinVar
Risk	rs397507872(-;-)
Alt	rs397507872(-;-)
Reference	Rs397507872(TG;TG)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32915127_32915128delGT
CLNSRC	ClinVar
CLNACC	RCV000045000.2,