rs587781321

Orientation

minus

Stabilized

minus

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

Make rs587781321(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61780325

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587781321
dbSNP (classic)	rs587781321
ClinGen	rs587781321
ebi	rs587781321
HLI	rs587781321
Exac	rs587781321
Gnomad	rs587781321
Varsome	rs587781321
LitVar	rs587781321
Map	rs587781321
PheGenI	rs587781321
Biobank	rs587781321
1000 genomes	rs587781321
hgdp	rs587781321
ensembl	rs587781321
geneview	rs587781321
scholar	rs587781321
google	rs587781321
pharmgkb	rs587781321
gwascentral	rs587781321
openSNP	rs587781321
23andMe	rs587781321
SNPshot	rs587781321
SNPdbe	rs587781321
MSV3d	rs587781321
GWAS Ctlg	rs587781321

Max Magnitude

6

ClinVar
Risk	rs587781321(A;A) rs587781321(T;T)
Alt	rs587781321(A;A) rs587781321(T;T)
Reference	Rs587781321(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast not specified Fanconi anemia Neoplasm of ovary not provided
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast not specified Fanconi anemia, complementation group J Neoplasm of ovary not provided
Reversed	1
HGVS	NC_000017.10:g.59857686G>A; NC_000017.10:g.59857686G>T
CLNSRC
CLNACC	RCV000166032.2, RCV000197937.1, RCV000284654.1, RCV000410706.1, RCV000411705.1, RCV000129060.4, RCV000228701.2, RCV000254651.2,