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rs863223777

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223777(C;T)
Make rs863223777(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114403757
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223777
dbSNP (classic)rs863223777
ClinGenrs863223777
ebirs863223777
HLIrs863223777
Exacrs863223777
Gnomadrs863223777
Varsomers863223777
LitVarrs863223777
Maprs863223777
PheGenIrs863223777
Biobankrs863223777
1000 genomesrs863223777
hgdprs863223777
ensemblrs863223777
geneviewrs863223777
scholarrs863223777
googlers863223777
pharmgkbrs863223777
gwascentralrs863223777
openSNPrs863223777
23andMers863223777
SNPshotrs863223777
SNPdbers863223777
MSV3drs863223777
GWAS Ctlgrs863223777
Max Magnitude0
ClinVar
Risk rs863223777(T;T)
Alt rs863223777(T;T)
Reference Rs863223777(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5 LOC101928456
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114841562G>A
CLNSRC
CLNACC RCV000200559.2,