rs1060501739

Orientation

minus

Stabilized

minus

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

Make rs1060501739(C;T)

Make rs1060501739(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

61784403

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs1060501739
dbSNP (classic)	rs1060501739
ClinGen	rs1060501739
ebi	rs1060501739
HLI	rs1060501739
Exac	rs1060501739
Gnomad	rs1060501739
Varsome	rs1060501739
LitVar	rs1060501739
Map	rs1060501739
PheGenI	rs1060501739
Biobank	rs1060501739
1000 genomes	rs1060501739
hgdp	rs1060501739
ensembl	rs1060501739
geneview	rs1060501739
scholar	rs1060501739
google	rs1060501739
pharmgkb	rs1060501739
gwascentral	rs1060501739
openSNP	rs1060501739
23andMe	rs1060501739
SNPshot	rs1060501739
SNPdbe	rs1060501739
MSV3d	rs1060501739
GWAS Ctlg	rs1060501739

Max Magnitude

0

ClinVar
Risk	rs1060501739(T;T)
Alt	rs1060501739(T;T)
Reference	Rs1060501739(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Fanconi anemia
Variation	info
Gene	BRIP1
CLNDBN	Familial cancer of breast Fanconi anemia, complementation group J
Reversed	1
HGVS	NC_000017.10:g.59861764G>A
CLNSRC
CLNACC	RCV000473198.1,