rs587780228

Orientation

minus

Stabilized

minus

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

Make rs587780228(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61793698

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587780228
dbSNP (classic)	rs587780228
ClinGen	rs587780228
ebi	rs587780228
HLI	rs587780228
Exac	rs587780228
Gnomad	rs587780228
Varsome	rs587780228
LitVar	rs587780228
Map	rs587780228
PheGenI	rs587780228
Biobank	rs587780228
1000 genomes	rs587780228
hgdp	rs587780228
ensembl	rs587780228
geneview	rs587780228
scholar	rs587780228
google	rs587780228
pharmgkb	rs587780228
gwascentral	rs587780228
openSNP	rs587780228
23andMe	rs587780228
SNPshot	rs587780228
SNPdbe	rs587780228
MSV3d	rs587780228
GWAS Ctlg	rs587780228

Max Magnitude

6

ClinVar
Risk	rs587780228(T;T)
Alt	rs587780228(T;T)
Reference	Rs587780228(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.59871059C>A
CLNSRC
CLNACC	RCV000116123.6, RCV000212309.3, RCV000473135.1,