rs587780224

Orientation

minus

Stabilized

minus

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

Make rs587780224(-;-)

Make rs587780224(-;CA)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61801266

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587780224
dbSNP (classic)	rs587780224
ClinGen	rs587780224
ebi	rs587780224
HLI	rs587780224
Exac	rs587780224
Gnomad	rs587780224
Varsome	rs587780224
LitVar	rs587780224
Map	rs587780224
PheGenI	rs587780224
Biobank	rs587780224
1000 genomes	rs587780224
hgdp	rs587780224
ensembl	rs587780224
geneview	rs587780224
scholar	rs587780224
google	rs587780224
pharmgkb	rs587780224
gwascentral	rs587780224
openSNP	rs587780224
23andMe	rs587780224
SNPshot	rs587780224
SNPdbe	rs587780224
MSV3d	rs587780224
GWAS Ctlg	rs587780224

Max Magnitude

0

ClinVar
Risk	rs587780224(-;-)
Alt	rs587780224(-;-)
Reference	Rs587780224(CA;CA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.59878627_59878628delTG
CLNSRC
CLNACC	RCV000116118.5,