rs397507698

Orientation

plus

Stabilized

plus

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

Make rs397507698(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338270

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507698
dbSNP (classic)	rs397507698
ClinGen	rs397507698
ebi	rs397507698
HLI	rs397507698
Exac	rs397507698
Gnomad	rs397507698
Varsome	rs397507698
LitVar	rs397507698
Map	rs397507698
PheGenI	rs397507698
Biobank	rs397507698
1000 genomes	rs397507698
hgdp	rs397507698
ensembl	rs397507698
geneview	rs397507698
scholar	rs397507698
google	rs397507698
pharmgkb	rs397507698
gwascentral	rs397507698
openSNP	rs397507698
23andMe	rs397507698
SNPshot	rs397507698
SNPdbe	rs397507698
MSV3d	rs397507698
GWAS Ctlg	rs397507698

Max Magnitude

6

ClinVar
Risk	rs397507698(-;-)
Alt	rs397507698(-;-)
Reference	Rs397507698(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912407delT
CLNSRC	ClinVar
CLNACC	RCV000044308.2, RCV000162054.3,