rs1060501757

Orientation

minus

Stabilized

minus

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

Make rs1060501757(G;T)

Make rs1060501757(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

61781006

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs1060501757
dbSNP (classic)	rs1060501757
ClinGen	rs1060501757
ebi	rs1060501757
HLI	rs1060501757
Exac	rs1060501757
Gnomad	rs1060501757
Varsome	rs1060501757
LitVar	rs1060501757
Map	rs1060501757
PheGenI	rs1060501757
Biobank	rs1060501757
1000 genomes	rs1060501757
hgdp	rs1060501757
ensembl	rs1060501757
geneview	rs1060501757
scholar	rs1060501757
google	rs1060501757
pharmgkb	rs1060501757
gwascentral	rs1060501757
openSNP	rs1060501757
23andMe	rs1060501757
SNPshot	rs1060501757
SNPdbe	rs1060501757
MSV3d	rs1060501757
GWAS Ctlg	rs1060501757

Max Magnitude

0

ClinVar
Risk	rs1060501757(T;T)
Alt	rs1060501757(T;T)
Reference	Rs1060501757(G;G)
Significance	Probable-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.59858367C>A
CLNSRC
CLNACC	RCV000468302.1,