rs876660613

Orientation

minus

Stabilized

minus

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

Make rs876660613(-;-)

Make rs876660613(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

61861494

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs876660613
dbSNP (classic)	rs876660613
ClinGen	rs876660613
ebi	rs876660613
HLI	rs876660613
Exac	rs876660613
Gnomad	rs876660613
Varsome	rs876660613
LitVar	rs876660613
Map	rs876660613
PheGenI	rs876660613
Biobank	rs876660613
1000 genomes	rs876660613
hgdp	rs876660613
ensembl	rs876660613
geneview	rs876660613
scholar	rs876660613
google	rs876660613
pharmgkb	rs876660613
gwascentral	rs876660613
openSNP	rs876660613
23andMe	rs876660613
SNPshot	rs876660613
SNPdbe	rs876660613
MSV3d	rs876660613
GWAS Ctlg	rs876660613

Max Magnitude

0

ClinVar
Risk	rs876660613(-;-)
Alt	rs876660613(-;-)
Reference	Rs876660613(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.59938855delA
CLNSRC
CLNACC	RCV000214696.1,