rs876660769

Orientation

minus

Stabilized

minus

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

Make rs876660769(-;-)

Make rs876660769(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

61847152

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs876660769
dbSNP (classic)	rs876660769
ClinGen	rs876660769
ebi	rs876660769
HLI	rs876660769
Exac	rs876660769
Gnomad	rs876660769
Varsome	rs876660769
LitVar	rs876660769
Map	rs876660769
PheGenI	rs876660769
Biobank	rs876660769
1000 genomes	rs876660769
hgdp	rs876660769
ensembl	rs876660769
geneview	rs876660769
scholar	rs876660769
google	rs876660769
pharmgkb	rs876660769
gwascentral	rs876660769
openSNP	rs876660769
23andMe	rs876660769
SNPshot	rs876660769
SNPdbe	rs876660769
MSV3d	rs876660769
GWAS Ctlg	rs876660769

Max Magnitude

0

ClinVar
Risk	rs876660769(-;-)
Alt	rs876660769(-;-)
Reference	Rs876660769(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.59924513delA
CLNSRC
CLNACC	RCV000217247.1,