rs786202610

Orientation

minus

Stabilized

minus

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

Make rs786202610(-;-)

Make rs786202610(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

61808495

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs786202610
dbSNP (classic)	rs786202610
ClinGen	rs786202610
ebi	rs786202610
HLI	rs786202610
Exac	rs786202610
Gnomad	rs786202610
Varsome	rs786202610
LitVar	rs786202610
Map	rs786202610
PheGenI	rs786202610
Biobank	rs786202610
1000 genomes	rs786202610
hgdp	rs786202610
ensembl	rs786202610
geneview	rs786202610
scholar	rs786202610
google	rs786202610
pharmgkb	rs786202610
gwascentral	rs786202610
openSNP	rs786202610
23andMe	rs786202610
SNPshot	rs786202610
SNPdbe	rs786202610
MSV3d	rs786202610
GWAS Ctlg	rs786202610

Max Magnitude

0

ClinVar
Risk	rs786202610(-;-)
Alt	rs786202610(-;-)
Reference	Rs786202610(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia not provided
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J not provided
Reversed	1
HGVS	NC_000017.10:g.59885856delT
CLNSRC
CLNACC	RCV000165504.1, RCV000168341.3, RCV000481880.1,