rs587781786

Orientation

minus

Stabilized

minus

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

Make rs587781786(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61849173

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587781786
dbSNP (classic)	rs587781786
ClinGen	rs587781786
ebi	rs587781786
HLI	rs587781786
Exac	rs587781786
Gnomad	rs587781786
Varsome	rs587781786
LitVar	rs587781786
Map	rs587781786
PheGenI	rs587781786
Biobank	rs587781786
1000 genomes	rs587781786
hgdp	rs587781786
ensembl	rs587781786
geneview	rs587781786
scholar	rs587781786
google	rs587781786
pharmgkb	rs587781786
gwascentral	rs587781786
openSNP	rs587781786
23andMe	rs587781786
SNPshot	rs587781786
SNPdbe	rs587781786
MSV3d	rs587781786
GWAS Ctlg	rs587781786

Max Magnitude

6

ClinVar
Risk	rs587781786(T;T)
Alt	rs587781786(T;T)
Reference	Rs587781786(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.59926534G>A
CLNSRC
CLNACC	RCV000130041.3, RCV000213568.1,