rs4986763

minus

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

Make rs4986763(C;C)

Make rs4986763(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

61683635

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs4986763
dbSNP (classic)	rs4986763
ClinGen	rs4986763
ebi	rs4986763
HLI	rs4986763
Exac	rs4986763
Gnomad	rs4986763
Varsome	rs4986763
LitVar	rs4986763
Map	rs4986763
PheGenI	rs4986763
Biobank	rs4986763
1000 genomes	rs4986763
hgdp	rs4986763
ensembl	rs4986763
geneview	rs4986763
scholar	rs4986763
google	rs4986763
pharmgkb	rs4986763
gwascentral	rs4986763
openSNP	rs4986763
23andMe	rs4986763
SNPshot	rs4986763
SNPdbe	rs4986763
MSV3d	rs4986763
GWAS Ctlg	rs4986763

GMAF

0.332

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 23473757] BRIP1 variations analysis reveals their relative importance as genetic susceptibility factor for cervical cancer

[PMID 19276285 ] Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.

[PMID 24301948] Further evidence for the contribution of the BRCA1-interacting protein-terminal helicase 1 (BRIP1) gene in breast cancer susceptibility

ClinVar
Risk	rs4986763(C;C)
Alt	rs4986763(C;C)
Reference	Rs4986763(T;T)
Significance	Probable-non-pathogenic
Disease	Hereditary cancer-predisposing syndrome not specified Fanconi anemia Neoplasm of breast Fanconi anemia Neoplasm of ovary
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome not specified Fanconi anemia Neoplasm of breast Fanconi anemia, complementation group J Neoplasm of ovary
Reversed	1
HGVS	NC_000017.10:g.59760996A>G
CLNSRC
CLNACC	RCV000162378.1, RCV000251677.1, RCV000283962.1, RCV000341269.1, RCV000410144.1, RCV000411217.1,