rs1060501779

Orientation

minus

Stabilized

minus

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

Make rs1060501779(-;-)

Make rs1060501779(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

61808753

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs1060501779
dbSNP (classic)	rs1060501779
ClinGen	rs1060501779
ebi	rs1060501779
HLI	rs1060501779
Exac	rs1060501779
Gnomad	rs1060501779
Varsome	rs1060501779
LitVar	rs1060501779
Map	rs1060501779
PheGenI	rs1060501779
Biobank	rs1060501779
1000 genomes	rs1060501779
hgdp	rs1060501779
ensembl	rs1060501779
geneview	rs1060501779
scholar	rs1060501779
google	rs1060501779
pharmgkb	rs1060501779
gwascentral	rs1060501779
openSNP	rs1060501779
23andMe	rs1060501779
SNPshot	rs1060501779
SNPdbe	rs1060501779
MSV3d	rs1060501779
GWAS Ctlg	rs1060501779

Max Magnitude

0

ClinVar
Risk	rs1060501779(-;-)
Alt	rs1060501779(-;-)
Reference	Rs1060501779(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.59886114delG
CLNSRC
CLNACC	RCV000463454.1,