rs771028677

Orientation

plus

Stabilized

plus

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

Make rs771028677(-;-)

Make rs771028677(-;TTTG)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

61684053

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs771028677
dbSNP (classic)	rs771028677
ClinGen	rs771028677
ebi	rs771028677
HLI	rs771028677
Exac	rs771028677
Gnomad	rs771028677
Varsome	rs771028677
LitVar	rs771028677
Map	rs771028677
PheGenI	rs771028677
Biobank	rs771028677
1000 genomes	rs771028677
hgdp	rs771028677
ensembl	rs771028677
geneview	rs771028677
scholar	rs771028677
google	rs771028677
pharmgkb	rs771028677
gwascentral	rs771028677
openSNP	rs771028677
23andMe	rs771028677
SNPshot	rs771028677
SNPdbe	rs771028677
MSV3d	rs771028677
GWAS Ctlg	rs771028677

Max Magnitude

0

ClinVar
Risk	rs771028677(-;-)
Alt	rs771028677(-;-)
Reference	Rs771028677(TTTG;TTTG)
Significance	Pathogenic
Disease	not provided Familial cancer of breast Fanconi anemia Hereditary cancer-predisposing syndrome Neoplasm of ovary
Variation	info
Gene	BRIP1
CLNDBN	not provided Familial cancer of breast Fanconi anemia, complementation group J Hereditary cancer-predisposing syndrome Neoplasm of ovary
Reversed	0
HGVS	NC_000017.10:g.59761414_59761417delTTTG
CLNSRC	Inc.
CLNACC	RCV000214087.2, RCV000230820.2, RCV000234901.1, RCV000410664.1, RCV000411728.1,