rs587780875

Orientation

minus

Stabilized

minus

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

Make rs587780875(C;C)

Make rs587780875(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

61793687

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587780875
dbSNP (classic)	rs587780875
ClinGen	rs587780875
ebi	rs587780875
HLI	rs587780875
Exac	rs587780875
Gnomad	rs587780875
Varsome	rs587780875
LitVar	rs587780875
Map	rs587780875
PheGenI	rs587780875
Biobank	rs587780875
1000 genomes	rs587780875
hgdp	rs587780875
ensembl	rs587780875
geneview	rs587780875
scholar	rs587780875
google	rs587780875
pharmgkb	rs587780875
gwascentral	rs587780875
openSNP	rs587780875
23andMe	rs587780875
SNPshot	rs587780875
SNPdbe	rs587780875
MSV3d	rs587780875
GWAS Ctlg	rs587780875

Max Magnitude

6

ClinVar
Risk	rs587780875(C;C) rs587780875(G;G)
Alt	rs587780875(C;C) rs587780875(G;G)
Reference	Rs587780875(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	BRIP1
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome not specified
Reversed	1
HGVS	NC_000017.10:g.59871048A>C; NC_000017.10:g.59871048A>G
CLNSRC
CLNACC	RCV000195948.1, RCV000124034.5, RCV000205219.1, RCV000212310.1,