rs1060501763

Orientation

minus

Stabilized

minus

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

Make rs1060501763(G;G)

Make rs1060501763(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

61859794

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs1060501763
dbSNP (classic)	rs1060501763
ClinGen	rs1060501763
ebi	rs1060501763
HLI	rs1060501763
Exac	rs1060501763
Gnomad	rs1060501763
Varsome	rs1060501763
LitVar	rs1060501763
Map	rs1060501763
PheGenI	rs1060501763
Biobank	rs1060501763
1000 genomes	rs1060501763
hgdp	rs1060501763
ensembl	rs1060501763
geneview	rs1060501763
scholar	rs1060501763
google	rs1060501763
pharmgkb	rs1060501763
gwascentral	rs1060501763
openSNP	rs1060501763
23andMe	rs1060501763
SNPshot	rs1060501763
SNPdbe	rs1060501763
MSV3d	rs1060501763
GWAS Ctlg	rs1060501763

Max Magnitude

0

ClinVar
Risk	rs1060501763(G;G)
Alt	rs1060501763(G;G)
Reference	Rs1060501763(T;T)
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.59937155A>C
CLNSRC
CLNACC	RCV000460534.1,