rs878853299

Orientation

plus

Stabilized

plus

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

Make rs878853299(TT;TT)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32338746

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs878853299
dbSNP (classic)	rs878853299
ClinGen	rs878853299
ebi	rs878853299
HLI	rs878853299
Exac	rs878853299
Gnomad	rs878853299
Varsome	rs878853299
LitVar	rs878853299
Map	rs878853299
PheGenI	rs878853299
Biobank	rs878853299
1000 genomes	rs878853299
hgdp	rs878853299
ensembl	rs878853299
geneview	rs878853299
scholar	rs878853299
google	rs878853299
pharmgkb	rs878853299
gwascentral	rs878853299
openSNP	rs878853299
23andMe	rs878853299
SNPshot	rs878853299
SNPdbe	rs878853299
MSV3d	rs878853299
GWAS Ctlg	rs878853299

Max Magnitude

6

ClinVar
Risk	rs878853299(TT;TT)
Alt	rs878853299(TT;TT)
Reference	Rs878853299(CTG;CTG)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912883_32912885delCTGinsTT
CLNSRC
CLNACC	RCV000225602.1,