rs397507600

Orientation

plus

Stabilized

plus

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

Make rs397507600(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32333148

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507600
dbSNP (classic)	rs397507600
ClinGen	rs397507600
ebi	rs397507600
HLI	rs397507600
Exac	rs397507600
Gnomad	rs397507600
Varsome	rs397507600
LitVar	rs397507600
Map	rs397507600
PheGenI	rs397507600
Biobank	rs397507600
1000 genomes	rs397507600
hgdp	rs397507600
ensembl	rs397507600
geneview	rs397507600
scholar	rs397507600
google	rs397507600
pharmgkb	rs397507600
gwascentral	rs397507600
openSNP	rs397507600
23andMe	rs397507600
SNPshot	rs397507600
SNPdbe	rs397507600
MSV3d	rs397507600
GWAS Ctlg	rs397507600

Max Magnitude

6

ClinVar
Risk	rs397507600(-;-)
Alt	rs397507600(-;-)
Reference	Rs397507600(TAATTGATAATGGA;TAATTGATAATGGA)
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.32907285_32907298delTAATTGATAATGGA
CLNSRC	ClinVar
CLNACC	RCV000043858.2, RCV000257260.2,