rs876659533

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Increased cancer risk; ovarian cancer & related

Make rs876659533(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

61776445

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs876659533
dbSNP (classic)	rs876659533
ClinGen	rs876659533
ebi	rs876659533
HLI	rs876659533
Exac	rs876659533
Gnomad	rs876659533
Varsome	rs876659533
LitVar	rs876659533
Map	rs876659533
PheGenI	rs876659533
Biobank	rs876659533
1000 genomes	rs876659533
hgdp	rs876659533
ensembl	rs876659533
geneview	rs876659533
scholar	rs876659533
google	rs876659533
pharmgkb	rs876659533
gwascentral	rs876659533
openSNP	rs876659533
23andMe	rs876659533
SNPshot	rs876659533
SNPdbe	rs876659533
MSV3d	rs876659533
GWAS Ctlg	rs876659533

Max Magnitude

6

ClinVar
Risk	rs876659533(T;T)
Alt	rs876659533(T;T)
Reference	Rs876659533(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.59853806G>A
CLNSRC
CLNACC	RCV000223392.1,