rs767234936

Orientation

plus

Stabilized

plus

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

Make rs767234936(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32338600

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs767234936
dbSNP (classic)	rs767234936
ClinGen	rs767234936
ebi	rs767234936
HLI	rs767234936
Exac	rs767234936
Gnomad	rs767234936
Varsome	rs767234936
LitVar	rs767234936
Map	rs767234936
PheGenI	rs767234936
Biobank	rs767234936
1000 genomes	rs767234936
hgdp	rs767234936
ensembl	rs767234936
geneview	rs767234936
scholar	rs767234936
google	rs767234936
pharmgkb	rs767234936
gwascentral	rs767234936
openSNP	rs767234936
23andMe	rs767234936
SNPshot	rs767234936
SNPdbe	rs767234936
MSV3d	rs767234936
GWAS Ctlg	rs767234936

Max Magnitude

6

ClinVar
Risk	rs767234936(-;-)
Alt	rs767234936(-;-)
Reference	Rs767234936(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912737delG
CLNSRC
CLNACC	RCV000219417.1, RCV000241053.1,