rs876660599

Orientation

plus

Stabilized

plus

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

Make rs876660599(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32380122

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876660599
dbSNP (classic)	rs876660599
ClinGen	rs876660599
ebi	rs876660599
HLI	rs876660599
Exac	rs876660599
Gnomad	rs876660599
Varsome	rs876660599
LitVar	rs876660599
Map	rs876660599
PheGenI	rs876660599
Biobank	rs876660599
1000 genomes	rs876660599
hgdp	rs876660599
ensembl	rs876660599
geneview	rs876660599
scholar	rs876660599
google	rs876660599
pharmgkb	rs876660599
gwascentral	rs876660599
openSNP	rs876660599
23andMe	rs876660599
SNPshot	rs876660599
SNPdbe	rs876660599
MSV3d	rs876660599
GWAS Ctlg	rs876660599

Max Magnitude

6

aka c.9233delT

ClinVar
Risk	rs876660599(-;-)
Alt	rs876660599(-;-)
Reference	Rs876660599(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32954259delT
CLNSRC
CLNACC	RCV000213244.1,