rs587780226

Orientation

minus

Stabilized

minus

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

Make rs587780226(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61799125

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587780226
dbSNP (classic)	rs587780226
ClinGen	rs587780226
ebi	rs587780226
HLI	rs587780226
Exac	rs587780226
Gnomad	rs587780226
Varsome	rs587780226
LitVar	rs587780226
Map	rs587780226
PheGenI	rs587780226
Biobank	rs587780226
1000 genomes	rs587780226
hgdp	rs587780226
ensembl	rs587780226
geneview	rs587780226
scholar	rs587780226
google	rs587780226
pharmgkb	rs587780226
gwascentral	rs587780226
openSNP	rs587780226
23andMe	rs587780226
SNPshot	rs587780226
SNPdbe	rs587780226
MSV3d	rs587780226
GWAS Ctlg	rs587780226

Max Magnitude

6

ClinVar
Risk	rs587780226(T;T)
Alt	rs587780226(T;T)
Reference	Rs587780226(C;C)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRIP1
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.59876486G>A
CLNSRC
CLNACC	RCV000116121.5, RCV000210150.1,