rs368796923

Orientation

plus

Stabilized

plus

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

Make rs368796923(A;A)

Reference

GRCh38 38.1/142

Chromosome

17

Position

61799200

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs368796923
dbSNP (classic)	rs368796923
ClinGen	rs368796923
ebi	rs368796923
HLI	rs368796923
Exac	rs368796923
Gnomad	rs368796923
Varsome	rs368796923
LitVar	rs368796923
Map	rs368796923
PheGenI	rs368796923
Biobank	rs368796923
1000 genomes	rs368796923
hgdp	rs368796923
ensembl	rs368796923
geneview	rs368796923
scholar	rs368796923
google	rs368796923
pharmgkb	rs368796923
gwascentral	rs368796923
openSNP	rs368796923
23andMe	rs368796923
SNPshot	rs368796923
SNPdbe	rs368796923
MSV3d	rs368796923
GWAS Ctlg	rs368796923

Max Magnitude

6

ClinVar
Risk	rs368796923(A;A)
Alt	rs368796923(A;A)
Reference	Rs368796923(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia Neoplasm of ovary not provided
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group J Neoplasm of ovary not provided
Reversed	0
HGVS	NC_000017.10:g.59876561G>A
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000129878.3, RCV000409609.1, RCV000411128.1, RCV000445256.1,