rs11079454

plus

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

Make rs11079454(A;A)

Make rs11079454(A;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

61679808

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs11079454
dbSNP (classic)	rs11079454
ClinGen	rs11079454
ebi	rs11079454
HLI	rs11079454
Exac	rs11079454
Gnomad	rs11079454
Varsome	rs11079454
LitVar	rs11079454
Map	rs11079454
PheGenI	rs11079454
Biobank	rs11079454
1000 genomes	rs11079454
hgdp	rs11079454
ensembl	rs11079454
geneview	rs11079454
scholar	rs11079454
google	rs11079454
pharmgkb	rs11079454
gwascentral	rs11079454
openSNP	rs11079454
23andMe	rs11079454
SNPshot	rs11079454
SNPdbe	rs11079454
MSV3d	rs11079454
GWAS Ctlg	rs11079454

GMAF

0.3843

Max Magnitude

0

?

(A;A) (A;T) (T;T)

28

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

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

ClinVar
Risk	rs11079454(A;A)
Alt	rs11079454(A;A)
Reference	Rs11079454(T;T)
Significance	Probable-non-pathogenic
Disease	Neoplasm of breast Fanconi anemia
Variation	info
Gene	BRIP1
CLNDBN	Neoplasm of breast Fanconi anemia
Reversed	0
HGVS	NC_000017.10:g.59757169T>A
CLNSRC
CLNACC	RCV000343111.1, RCV000379026.1,