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rs8176323

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs8176323(C;G)
Make rs8176323(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position43043694
is asnp
is mentioned by
dbSNPrs8176323
ebirs8176323
HLIrs8176323
Exacrs8176323
Varsomers8176323
Maprs8176323
PheGenIrs8176323
hapmaprs8176323
1000 genomesrs8176323
hgdprs8176323
ensemblrs8176323
gopubmedrs8176323
geneviewrs8176323
scholarrs8176323
googlers8176323
pharmgkbrs8176323
gwascentralrs8176323
openSNPrs8176323
23andMers8176323
23andMe allrs8176323
SNP Nexus

SNPshotrs8176323
SNPdbers8176323
MSV3drs8176323
GWAS Ctlgrs8176323
Max Magnitude0
? (C;C) (C;G) (G;G) 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 rs8176323(G;G)
Alt rs8176323(G;G)
Reference rs8176323(C;C)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41195711G>C
CLNSRC
CLNACC RCV000191173.1,