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rs863223781

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223781(G;T)
Make rs863223781(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114401821
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223781
ebirs863223781
HLIrs863223781
Exacrs863223781
Varsomers863223781
Maprs863223781
PheGenIrs863223781
hapmaprs863223781
1000 genomesrs863223781
hgdprs863223781
ensemblrs863223781
gopubmedrs863223781
geneviewrs863223781
scholarrs863223781
googlers863223781
pharmgkbrs863223781
gwascentralrs863223781
openSNPrs863223781
23andMers863223781
23andMe allrs863223781
SNP Nexus

SNPshotrs863223781
SNPdbers863223781
MSV3drs863223781
GWAS Ctlgrs863223781
Max Magnitude0
ClinVar
Risk rs863223781(T;T)
Alt rs863223781(T;T)
Reference rs863223781(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114839626C>A
CLNSRC
CLNACC RCV000197866.1,