rs276174915

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AAGATTCAGGT;AAGATTCAGGT)	0	common in clinvar
(ATTCAGGTAAG;ATTCAGGTAAG)	0	common/normal

Make rs276174915(-;-)

Make rs276174915(-;ATTCAGGTAAG)

Reference

GRCh38 38.1/142

Chromosome

13

Position

32379510

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174915
dbSNP (classic)	rs276174915
ClinGen	rs276174915
ebi	rs276174915
HLI	rs276174915
Exac	rs276174915
Gnomad	rs276174915
Varsome	rs276174915
LitVar	rs276174915
Map	rs276174915
PheGenI	rs276174915
Biobank	rs276174915
1000 genomes	rs276174915
hgdp	rs276174915
ensembl	rs276174915
geneview	rs276174915
scholar	rs276174915
google	rs276174915
pharmgkb	rs276174915
gwascentral	rs276174915
openSNP	rs276174915
23andMe	rs276174915
SNPshot	rs276174915
SNPdbe	rs276174915
MSV3d	rs276174915
GWAS Ctlg	rs276174915

Max Magnitude

0

ClinVar
Risk	rs276174915(-;-)
Alt	rs276174915(-;-)
Reference	Rs276174915(AAGATTCAGGT;AAGATTCAGGT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome not provided Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32953647_32953657delATTCAGGTAAG
CLNSRC	Ambry Genetics
CLNACC	RCV000129964.2, RCV000236901.1, RCV000238747.2,