rs28897758

Orientation

plus

Stabilized

plus

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

Make rs28897758(G;G)

Make rs28897758(G;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394734

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs28897758
dbSNP (classic)	rs28897758
ClinGen	rs28897758
ebi	rs28897758
HLI	rs28897758
Exac	rs28897758
Gnomad	rs28897758
Varsome	rs28897758
LitVar	rs28897758
Map	rs28897758
PheGenI	rs28897758
Biobank	rs28897758
1000 genomes	rs28897758
hgdp	rs28897758
ensembl	rs28897758
geneview	rs28897758
scholar	rs28897758
google	rs28897758
pharmgkb	rs28897758
gwascentral	rs28897758
openSNP	rs28897758
23andMe	rs28897758
SNPshot	rs28897758
SNPdbe	rs28897758
MSV3d	rs28897758
GWAS Ctlg	rs28897758

Max Magnitude

0

ClinVar
Risk	rs28897758(C;C) rs28897758(G;G)
Alt	rs28897758(C;C) rs28897758(G;G)
Reference	Rs28897758(T;T)
Significance	Untested
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000013.10:g.32968871T>C; NC_000013.10:g.32968871T>G
CLNSRC	ClinVar
CLNACC	RCV000198262.1, RCV000031813.5, RCV000045787.4, RCV000162632.2, RCV000485324.1,