rs786203717

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;AAGA)	6	Ovarian cancer susceptibility
(AAGA;AAGA)	0	common in clinvar

Make rs786203717(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

61684051

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs786203717
dbSNP (classic)	rs786203717
ClinGen	rs786203717
ebi	rs786203717
HLI	rs786203717
Exac	rs786203717
Gnomad	rs786203717
Varsome	rs786203717
LitVar	rs786203717
Map	rs786203717
PheGenI	rs786203717
Biobank	rs786203717
1000 genomes	rs786203717
hgdp	rs786203717
ensembl	rs786203717
geneview	rs786203717
scholar	rs786203717
google	rs786203717
pharmgkb	rs786203717
gwascentral	rs786203717
openSNP	rs786203717
23andMe	rs786203717
SNPshot	rs786203717
SNPdbe	rs786203717
MSV3d	rs786203717
GWAS Ctlg	rs786203717

Max Magnitude

6

ClinVar
Risk	rs786203717(-;-)
Alt	rs786203717(-;-)
Reference	Rs786203717(AAGA;AAGA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia not provided
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J not provided
Reversed	1
HGVS	NC_000017.10:g.59761412_59761415delTCTT
CLNSRC
CLNACC	RCV000167141.1, RCV000458808.1, RCV000478533.1,