rs1060501778

Orientation

minus

Stabilized

minus

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

Make rs1060501778(-;-)

Make rs1060501778(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

61847180

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs1060501778
dbSNP (classic)	rs1060501778
ClinGen	rs1060501778
ebi	rs1060501778
HLI	rs1060501778
Exac	rs1060501778
Gnomad	rs1060501778
Varsome	rs1060501778
LitVar	rs1060501778
Map	rs1060501778
PheGenI	rs1060501778
Biobank	rs1060501778
1000 genomes	rs1060501778
hgdp	rs1060501778
ensembl	rs1060501778
geneview	rs1060501778
scholar	rs1060501778
google	rs1060501778
pharmgkb	rs1060501778
gwascentral	rs1060501778
openSNP	rs1060501778
23andMe	rs1060501778
SNPshot	rs1060501778
SNPdbe	rs1060501778
MSV3d	rs1060501778
GWAS Ctlg	rs1060501778

Max Magnitude

0

ClinVar
Risk	rs1060501778(-;-)
Alt	rs1060501778(-;-)
Reference	Rs1060501778(T;T)
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.59924541delA
CLNSRC
CLNACC	RCV000475128.1,