rs568027879

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs568027879(A;A)

Make rs568027879(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32329440

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs568027879
dbSNP (classic)	rs568027879
ClinGen	rs568027879
ebi	rs568027879
HLI	rs568027879
Exac	rs568027879
Gnomad	rs568027879
Varsome	rs568027879
LitVar	rs568027879
Map	rs568027879
PheGenI	rs568027879
Biobank	rs568027879
1000 genomes	rs568027879
hgdp	rs568027879
ensembl	rs568027879
geneview	rs568027879
scholar	rs568027879
google	rs568027879
pharmgkb	rs568027879
gwascentral	rs568027879
openSNP	rs568027879
23andMe	rs568027879
SNPshot	rs568027879
SNPdbe	rs568027879
MSV3d	rs568027879
GWAS Ctlg	rs568027879

Max Magnitude

0

ClinVar
Risk	rs568027879(A;A) rs568027879(G;G)
Alt	rs568027879(A;A) rs568027879(G;G)
Reference	Rs568027879(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not specified
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 not specified
Reversed	0
HGVS	NC_000013.10:g.32903577C>A; NC_000013.10:g.32903577C>G
CLNSRC
CLNACC	RCV000165268.2, RCV000464025.1, RCV000204368.2, RCV000220060.1, RCV000238832.1, RCV000481337.1,