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rs1061651

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1061651(A;G)
Make rs1061651(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114670556
GeneTBX3
is asnp
is mentioned by
dbSNPrs1061651
dbSNP (classic)rs1061651
ClinGenrs1061651
ebirs1061651
HLIrs1061651
Exacrs1061651
Gnomadrs1061651
Varsomers1061651
LitVarrs1061651
Maprs1061651
PheGenIrs1061651
Biobankrs1061651
1000 genomesrs1061651
hgdprs1061651
ensemblrs1061651
geneviewrs1061651
scholarrs1061651
googlers1061651
pharmgkbrs1061651
gwascentralrs1061651
openSNPrs1061651
23andMers1061651
SNPshotrs1061651
SNPdbers1061651
MSV3drs1061651
GWAS Ctlgrs1061651
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 rs1061651(G;G)
Alt rs1061651(G;G)
Reference Rs1061651(A;A)
Significance Non-pathogenic
Disease Ulnar-mammary syndrome
Variation info
Gene TBX3
CLNDBN Ulnar-mammary syndrome
Reversed 1
HGVS NC_000012.11:g.115108361T>C
CLNSRC
CLNACC RCV000319833.1,