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rs8176199

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs8176199(A;C)
Make rs8176199(C;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position43078507
GeneBRCA1
is asnp
is mentioned by
dbSNPrs8176199
ebirs8176199
HLIrs8176199
Exacrs8176199
Varsomers8176199
Maprs8176199
PheGenIrs8176199
hapmaprs8176199
1000 genomesrs8176199
hgdprs8176199
ensemblrs8176199
gopubmedrs8176199
geneviewrs8176199
scholarrs8176199
googlers8176199
pharmgkbrs8176199
gwascentralrs8176199
openSNPrs8176199
23andMers8176199
23andMe allrs8176199
SNP Nexus

SNPshotrs8176199
SNPdbers8176199
MSV3drs8176199
GWAS Ctlgrs8176199
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 rs8176199(C;C)
Alt rs8176199(C;C)
Reference rs8176199(A;A)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41230524T>G
CLNSRC
CLNACC RCV000191337.1,