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rs863223786

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223786(-;A)
Make rs863223786(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114394792
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223786
dbSNP (old)rs863223786
ClinGenrs863223786
ebirs863223786
HLIrs863223786
Exacrs863223786
Varsomers863223786
Maprs863223786
PheGenIrs863223786
Biobankrs863223786
1000 genomesrs863223786
hgdprs863223786
ensemblrs863223786
gopubmedrs863223786
geneviewrs863223786
scholarrs863223786
googlers863223786
pharmgkbrs863223786
gwascentralrs863223786
openSNPrs863223786
23andMers863223786
23andMe allrs863223786
SNP Nexus

SNPshotrs863223786
SNPdbers863223786
MSV3drs863223786
GWAS Ctlgrs863223786
Max Magnitude0
ClinVar
Risk rs863223786(A;A)
Alt rs863223786(A;A)
Reference Rs863223786(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114832598dupT
CLNSRC
CLNACC RCV000197595.1,