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rs2070833

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2070833(A;A)
Make rs2070833(A;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position43090832
GeneBRCA1
is asnp
is mentioned by
dbSNPrs2070833
ebirs2070833
HLIrs2070833
Exacrs2070833
Varsomers2070833
Maprs2070833
PheGenIrs2070833
hapmaprs2070833
1000 genomesrs2070833
hgdprs2070833
ensemblrs2070833
gopubmedrs2070833
geneviewrs2070833
scholarrs2070833
googlers2070833
pharmgkbrs2070833
gwascentralrs2070833
openSNPrs2070833
23andMers2070833
23andMe allrs2070833
SNP Nexus

SNPshotrs2070833
SNPdbers2070833
MSV3drs2070833
GWAS Ctlgrs2070833
Max Magnitude0
? (A;A) (A;C) (C;C) 28

[PMID 25463638] Association of genetic polymorphisms in AURKA, BRCA1, CCNE1 and CDK2 with the risk of endometrial carcinoma and clinicopathological parameters among Chinese Han women

ClinVar
Risk rs2070833(A;A)
Alt rs2070833(A;A)
Reference rs2070833(C;C)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41242849G>T
CLNSRC
CLNACC RCV000191388.1,