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rs8853

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs8853(A;G)
Make rs8853(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114671102
GeneTBX3
is asnp
is mentioned by
dbSNPrs8853
dbSNP (old)rs8853
ClinGenrs8853
ebirs8853
HLIrs8853
Exacrs8853
Gnomadrs8853
Varsomers8853
Maprs8853
PheGenIrs8853
Biobankrs8853
1000 genomesrs8853
hgdprs8853
ensemblrs8853
gopubmedrs8853
geneviewrs8853
scholarrs8853
googlers8853
pharmgkbrs8853
gwascentralrs8853
openSNPrs8853
23andMers8853
23andMe allrs8853
SNP Nexus

SNPshotrs8853
SNPdbers8853
MSV3drs8853
GWAS Ctlgrs8853
Max Magnitude0

[PMID 26920143OA-icon.png] Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.


ClinVar
Risk rs8853(G;G)
Alt rs8853(G;G)
Reference Rs8853(A;A)
Significance Non-pathogenic
Disease Ulnar-mammary syndrome
Variation info
Gene TBX3
CLNDBN Ulnar-mammary syndrome
Reversed 1
HGVS NC_000012.11:g.115108907T>C
CLNSRC
CLNACC RCV000398645.1,