rs80359153

Orientation

plus

Stabilized

plus

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

Make rs80359153(A;T)

Make rs80359153(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379802

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359153
dbSNP (classic)	rs80359153
ClinGen	rs80359153
ebi	rs80359153
HLI	rs80359153
Exac	rs80359153
Gnomad	rs80359153
Varsome	rs80359153
LitVar	rs80359153
Map	rs80359153
PheGenI	rs80359153
Biobank	rs80359153
1000 genomes	rs80359153
hgdp	rs80359153
ensembl	rs80359153
geneview	rs80359153
scholar	rs80359153
google	rs80359153
pharmgkb	rs80359153
gwascentral	rs80359153
openSNP	rs80359153
23andMe	rs80359153
SNPshot	rs80359153
SNPdbe	rs80359153
MSV3d	rs80359153
GWAS Ctlg	rs80359153

Max Magnitude

0

ClinVar
Risk	rs80359153(T;T)
Alt	rs80359153(T;T)
Reference	Rs80359153(A;A)
Significance	Other
Disease	Hereditary breast and ovarian cancer syndrome not specified Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome not specified Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32953939A>T
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000045686.3, RCV000074558.7, RCV000083151.4, RCV000129004.3,