rs876659977

Orientation

plus

Stabilized

plus

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

Make rs876659977(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32338532

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876659977
dbSNP (classic)	rs876659977
ClinGen	rs876659977
ebi	rs876659977
HLI	rs876659977
Exac	rs876659977
Gnomad	rs876659977
Varsome	rs876659977
LitVar	rs876659977
Map	rs876659977
PheGenI	rs876659977
Biobank	rs876659977
1000 genomes	rs876659977
hgdp	rs876659977
ensembl	rs876659977
geneview	rs876659977
scholar	rs876659977
google	rs876659977
pharmgkb	rs876659977
gwascentral	rs876659977
openSNP	rs876659977
23andMe	rs876659977
SNPshot	rs876659977
SNPdbe	rs876659977
MSV3d	rs876659977
GWAS Ctlg	rs876659977

Max Magnitude

6

aka c.4177dupG

ClinVar
Risk	rs876659977(G;G)
Alt	rs876659977(G;G)
Reference	Rs876659977(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32912669dupG
CLNSRC
CLNACC	RCV000214720.1,