rs587782410

Orientation

minus

Stabilized

minus

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

Make rs587782410(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61685976

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587782410
dbSNP (classic)	rs587782410
ClinGen	rs587782410
ebi	rs587782410
HLI	rs587782410
Exac	rs587782410
Gnomad	rs587782410
Varsome	rs587782410
LitVar	rs587782410
Map	rs587782410
PheGenI	rs587782410
Biobank	rs587782410
1000 genomes	rs587782410
hgdp	rs587782410
ensembl	rs587782410
geneview	rs587782410
scholar	rs587782410
google	rs587782410
pharmgkb	rs587782410
gwascentral	rs587782410
openSNP	rs587782410
23andMe	rs587782410
SNPshot	rs587782410
SNPdbe	rs587782410
MSV3d	rs587782410
GWAS Ctlg	rs587782410

Max Magnitude

6

ClinVar
Risk	rs587782410(G;G)
Alt	rs587782410(G;G)
Reference	Rs587782410(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Fanconi anemia Neoplasm of ovary Familial cancer of breast
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome not provided Fanconi anemia, complementation group J Neoplasm of ovary Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.59763337A>C
CLNSRC
CLNACC	RCV000131449.2, RCV000216847.3, RCV000410978.1, RCV000412207.1, RCV000468535.1,