rs587781985

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs587781985(-;G)

Make rs587781985(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61780342

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587781985
dbSNP (classic)	rs587781985
ClinGen	rs587781985
ebi	rs587781985
HLI	rs587781985
Exac	rs587781985
Gnomad	rs587781985
Varsome	rs587781985
LitVar	rs587781985
Map	rs587781985
PheGenI	rs587781985
Biobank	rs587781985
1000 genomes	rs587781985
hgdp	rs587781985
ensembl	rs587781985
geneview	rs587781985
scholar	rs587781985
google	rs587781985
pharmgkb	rs587781985
gwascentral	rs587781985
openSNP	rs587781985
23andMe	rs587781985
SNPshot	rs587781985
SNPdbe	rs587781985
MSV3d	rs587781985
GWAS Ctlg	rs587781985

Max Magnitude

0

ClinVar
Risk	rs587781985(G;G)
Alt	rs587781985(G;G)
Reference	Rs587781985(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Neoplasm of ovary Fanconi anemia
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome Neoplasm of ovary Fanconi anemia, complementation group J
Reversed	1
HGVS	NC_000017.10:g.59857703_59857704insC
CLNSRC
CLNACC	RCV000130385.3, RCV000409999.1, RCV000412318.1,