rs864622277

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;G)	6	Ovarian cancer susceptibility
(G;G)	0	common in clinvar

Make rs864622277(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

61847221

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs864622277
dbSNP (classic)	rs864622277
ClinGen	rs864622277
ebi	rs864622277
HLI	rs864622277
Exac	rs864622277
Gnomad	rs864622277
Varsome	rs864622277
LitVar	rs864622277
Map	rs864622277
PheGenI	rs864622277
Biobank	rs864622277
1000 genomes	rs864622277
hgdp	rs864622277
ensembl	rs864622277
geneview	rs864622277
scholar	rs864622277
google	rs864622277
pharmgkb	rs864622277
gwascentral	rs864622277
openSNP	rs864622277
23andMe	rs864622277
SNPshot	rs864622277
SNPdbe	rs864622277
MSV3d	rs864622277
GWAS Ctlg	rs864622277

Max Magnitude

6

aka c.508-1G>C

Considered likely pathogenic in ClinVar for hereditary cancer (breast)

23andMe name: i709076

ClinVar
Risk	rs864622277(C;C)
Alt	rs864622277(C;C)
Reference	Rs864622277(G;G)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRIP1
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.59924582C>G
CLNSRC
CLNACC	RCV000203783.1, RCV000449088.1,