rs587780236

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;T)	6	Increased cancer risk; ovarian cancer & related

Make rs587780236(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61743118

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs587780236
dbSNP (classic)	rs587780236
ClinGen	rs587780236
ebi	rs587780236
HLI	rs587780236
Exac	rs587780236
Gnomad	rs587780236
Varsome	rs587780236
LitVar	rs587780236
Map	rs587780236
PheGenI	rs587780236
Biobank	rs587780236
1000 genomes	rs587780236
hgdp	rs587780236
ensembl	rs587780236
geneview	rs587780236
scholar	rs587780236
google	rs587780236
pharmgkb	rs587780236
gwascentral	rs587780236
openSNP	rs587780236
23andMe	rs587780236
SNPshot	rs587780236
SNPdbe	rs587780236
MSV3d	rs587780236
GWAS Ctlg	rs587780236

Max Magnitude

6

aka c.2273dupT (p.Ala759Serfs)

ClinVar
Risk	rs587780236(T;T)
Alt	rs587780236(T;T)
Reference	Rs587780236(-;-)
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.59820480dupA
CLNSRC
CLNACC	RCV000116138.4, RCV000258967.1,