rs587781655

Orientation

minus

Stabilized

minus

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

Make rs587781655(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61808466

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587781655
dbSNP (classic)	rs587781655
ClinGen	rs587781655
ebi	rs587781655
HLI	rs587781655
Exac	rs587781655
Gnomad	rs587781655
Varsome	rs587781655
LitVar	rs587781655
Map	rs587781655
PheGenI	rs587781655
Biobank	rs587781655
1000 genomes	rs587781655
hgdp	rs587781655
ensembl	rs587781655
geneview	rs587781655
scholar	rs587781655
google	rs587781655
pharmgkb	rs587781655
gwascentral	rs587781655
openSNP	rs587781655
23andMe	rs587781655
SNPshot	rs587781655
SNPdbe	rs587781655
MSV3d	rs587781655
GWAS Ctlg	rs587781655

Max Magnitude

6

ClinVar
Risk	rs587781655(A;A)
Alt	rs587781655(A;A)
Reference	Rs587781655(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast Fanconi anemia
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast Fanconi anemia, complementation group J
Reversed	1
HGVS	NC_000017.10:g.59885827C>T
CLNSRC
CLNACC	RCV000129793.3, RCV000434292.1, RCV000472419.1,