rs28897751

Orientation

plus

Stabilized

plus

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

Make rs28897751(C;C)

Make rs28897751(C;T)

Reference

GRCh38 38.1/142

Chromosome

13

Position

32370445

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs28897751
dbSNP (classic)	rs28897751
ClinGen	rs28897751
ebi	rs28897751
HLI	rs28897751
Exac	rs28897751
Gnomad	rs28897751
Varsome	rs28897751
LitVar	rs28897751
Map	rs28897751
PheGenI	rs28897751
Biobank	rs28897751
1000 genomes	rs28897751
hgdp	rs28897751
ensembl	rs28897751
geneview	rs28897751
scholar	rs28897751
google	rs28897751
pharmgkb	rs28897751
gwascentral	rs28897751
openSNP	rs28897751
23andMe	rs28897751
SNPshot	rs28897751
SNPdbe	rs28897751
MSV3d	rs28897751
GWAS Ctlg	rs28897751

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	rs28897751(C;C)
Alt	rs28897751(C;C)
Reference	Rs28897751(T;T)
Significance	Untested
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32944582T>C
CLNSRC	ClinVar
CLNACC	RCV000045498.2, RCV000113921.1,