rs80358702

Orientation

plus

Stabilized

plus

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

Make rs80358702(A;A)

Make rs80358702(A;G)

Reference

GRCh38 38.1/142

Chromosome

13

Position

32326150

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80358702
dbSNP (classic)	rs80358702
ClinGen	rs80358702
ebi	rs80358702
HLI	rs80358702
Exac	rs80358702
Gnomad	rs80358702
Varsome	rs80358702
LitVar	rs80358702
Map	rs80358702
PheGenI	rs80358702
Biobank	rs80358702
1000 genomes	rs80358702
hgdp	rs80358702
ensembl	rs80358702
geneview	rs80358702
scholar	rs80358702
google	rs80358702
pharmgkb	rs80358702
gwascentral	rs80358702
openSNP	rs80358702
23andMe	rs80358702
SNPshot	rs80358702
SNPdbe	rs80358702
MSV3d	rs80358702
GWAS Ctlg	rs80358702

Max Magnitude

0

ClinVar
Risk	rs80358702(A;A)
Alt	rs80358702(A;A)
Reference	Rs80358702(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32900287G>A
CLNSRC	ClinVar
CLNACC	RCV000044486.2, RCV000113649.1, RCV000218417.1, RCV000236273.1,