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rs863223773

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223773(C;C)
Make rs863223773(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114398710
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223773
ebirs863223773
HLIrs863223773
Exacrs863223773
Varsomers863223773
Maprs863223773
PheGenIrs863223773
hapmaprs863223773
1000 genomesrs863223773
hgdprs863223773
ensemblrs863223773
gopubmedrs863223773
geneviewrs863223773
scholarrs863223773
googlers863223773
pharmgkbrs863223773
gwascentralrs863223773
openSNPrs863223773
23andMers863223773
23andMe allrs863223773
SNP Nexus

SNPshotrs863223773
SNPdbers863223773
MSV3drs863223773
GWAS Ctlgrs863223773
Max Magnitude0
ClinVar
Risk rs863223773(C;C)
Alt rs863223773(C;C)
Reference rs863223773(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114836515C>G
CLNSRC
CLNACC RCV000200855.1,