rs730881633

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Ovarian cancer susceptibility

Make rs730881633(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61801327

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs730881633
dbSNP (classic)	rs730881633
ClinGen	rs730881633
ebi	rs730881633
HLI	rs730881633
Exac	rs730881633
Gnomad	rs730881633
Varsome	rs730881633
LitVar	rs730881633
Map	rs730881633
PheGenI	rs730881633
Biobank	rs730881633
1000 genomes	rs730881633
hgdp	rs730881633
ensembl	rs730881633
geneview	rs730881633
scholar	rs730881633
google	rs730881633
pharmgkb	rs730881633
gwascentral	rs730881633
openSNP	rs730881633
23andMe	rs730881633
SNPshot	rs730881633
SNPdbe	rs730881633
MSV3d	rs730881633
GWAS Ctlg	rs730881633

Max Magnitude

6

ClinVar
Risk	rs730881633(T;T)
Alt	rs730881633(T;T)
Reference	Rs730881633(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.59878688G>A
CLNSRC
CLNACC	RCV000160335.3, RCV000212307.2,