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rs11079454

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs11079454(A;A)
Make rs11079454(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position61679808
GeneBRIP1
is asnp
is mentioned by
dbSNPrs11079454
dbSNP (old)rs11079454
ClinGenrs11079454
ebirs11079454
HLIrs11079454
Exacrs11079454
Gnomadrs11079454
Varsomers11079454
Maprs11079454
PheGenIrs11079454
Biobankrs11079454
1000 genomesrs11079454
hgdprs11079454
ensemblrs11079454
gopubmedrs11079454
geneviewrs11079454
scholarrs11079454
googlers11079454
pharmgkbrs11079454
gwascentralrs11079454
openSNPrs11079454
23andMers11079454
23andMe allrs11079454
SNP Nexus

SNPshotrs11079454
SNPdbers11079454
MSV3drs11079454
GWAS Ctlgrs11079454
GMAF0.3843
Max Magnitude0
? (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,