rs876658425

Orientation

plus

Stabilized

plus

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

Make rs876658425(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32340622

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876658425
dbSNP (classic)	rs876658425
ClinGen	rs876658425
ebi	rs876658425
HLI	rs876658425
Exac	rs876658425
Gnomad	rs876658425
Varsome	rs876658425
LitVar	rs876658425
Map	rs876658425
PheGenI	rs876658425
Biobank	rs876658425
1000 genomes	rs876658425
hgdp	rs876658425
ensembl	rs876658425
geneview	rs876658425
scholar	rs876658425
google	rs876658425
pharmgkb	rs876658425
gwascentral	rs876658425
openSNP	rs876658425
23andMe	rs876658425
SNPshot	rs876658425
SNPdbe	rs876658425
MSV3d	rs876658425
GWAS Ctlg	rs876658425

Max Magnitude

6

aka c.6267_6274delGCATAGTC

ClinVar
Risk	rs876658425(-;-)
Alt	rs876658425(-;-)
Reference	Rs876658425(GCATAGTC;GCATAGTC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32914759_32914766delGCATAGTC
CLNSRC
CLNACC	RCV000216272.1,