rs786203429

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(ATA;ATA)	0	common in clinvar
(ATA;CT)	6	Ovarian cancer susceptibility

Make rs786203429(CT;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

61849196

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs786203429
dbSNP (classic)	rs786203429
ClinGen	rs786203429
ebi	rs786203429
HLI	rs786203429
Exac	rs786203429
Gnomad	rs786203429
Varsome	rs786203429
LitVar	rs786203429
Map	rs786203429
PheGenI	rs786203429
Biobank	rs786203429
1000 genomes	rs786203429
hgdp	rs786203429
ensembl	rs786203429
geneview	rs786203429
scholar	rs786203429
google	rs786203429
pharmgkb	rs786203429
gwascentral	rs786203429
openSNP	rs786203429
23andMe	rs786203429
SNPshot	rs786203429
SNPdbe	rs786203429
MSV3d	rs786203429
GWAS Ctlg	rs786203429

Max Magnitude

6

aka c.438_440delATAinsCT

ClinVar
Risk	rs786203429(CT;CT)
Alt	rs786203429(CT;CT)
Reference	Rs786203429(ATA;ATA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.59926557_59926559delTATinsAG
CLNSRC
CLNACC	RCV000166730.2,