rs397507903

Orientation

plus

Stabilized

plus

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

Make rs397507903(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32319080

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507903
dbSNP (classic)	rs397507903
ClinGen	rs397507903
ebi	rs397507903
HLI	rs397507903
Exac	rs397507903
Gnomad	rs397507903
Varsome	rs397507903
LitVar	rs397507903
Map	rs397507903
PheGenI	rs397507903
Biobank	rs397507903
1000 genomes	rs397507903
hgdp	rs397507903
ensembl	rs397507903
geneview	rs397507903
scholar	rs397507903
google	rs397507903
pharmgkb	rs397507903
gwascentral	rs397507903
openSNP	rs397507903
23andMe	rs397507903
SNPshot	rs397507903
SNPdbe	rs397507903
MSV3d	rs397507903
GWAS Ctlg	rs397507903

Max Magnitude

6

ClinVar
Risk	rs397507903(-;-)
Alt	rs397507903(-;-)
Reference	Rs397507903(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32893217delT
CLNSRC	ClinVar
CLNACC	RCV000045163.2, RCV000166421.1, RCV000241037.2,