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rs799906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs799906(C;C)
Make rs799906(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43126099
GeneBRCA1
is asnp
is mentioned by
dbSNPrs799906
ebirs799906
HLIrs799906
Exacrs799906
Varsomers799906
Maprs799906
PheGenIrs799906
hapmaprs799906
1000 genomesrs799906
hgdprs799906
ensemblrs799906
gopubmedrs799906
geneviewrs799906
scholarrs799906
googlers799906
pharmgkbrs799906
gwascentralrs799906
openSNPrs799906
23andMers799906
23andMe allrs799906
SNP Nexus

SNPshotrs799906
SNPdbers799906
MSV3drs799906
GWAS Ctlgrs799906
GMAF0.4481
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 12466288OA-icon.png] Haplotype and linkage disequilibrium architecture for human cancer-associated genes.


GET Evidence
rs799906
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.507936
summary



ClinVar
Risk rs799906(C;C)
Alt rs799906(C;C)
Reference rs799906(T;T)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene NBR2 BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 0
HGVS NC_000017.10:g.41278116T>C
CLNSRC
CLNACC RCV000191528.1,