rs752309409

Orientation

plus

Stabilized

plus

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

Make rs752309409(A;A)

Make rs752309409(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

61808634

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs752309409
dbSNP (classic)	rs752309409
ClinGen	rs752309409
ebi	rs752309409
HLI	rs752309409
Exac	rs752309409
Gnomad	rs752309409
Varsome	rs752309409
LitVar	rs752309409
Map	rs752309409
PheGenI	rs752309409
Biobank	rs752309409
1000 genomes	rs752309409
hgdp	rs752309409
ensembl	rs752309409
geneview	rs752309409
scholar	rs752309409
google	rs752309409
pharmgkb	rs752309409
gwascentral	rs752309409
openSNP	rs752309409
23andMe	rs752309409
SNPshot	rs752309409
SNPdbe	rs752309409
MSV3d	rs752309409
GWAS Ctlg	rs752309409

Max Magnitude

0

ClinVar
Risk	rs752309409(A;A)
Alt	rs752309409(A;A)
Reference	Rs752309409(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed	0
HGVS	NC_000017.10:g.59885995G>A
CLNSRC
CLNACC	RCV000165345.2, RCV000206065.1, RCV000219928.1,