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rs863223775

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223775(C;T)
Make rs863223775(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114398617
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223775
ebirs863223775
HLIrs863223775
Exacrs863223775
Varsomers863223775
Maprs863223775
PheGenIrs863223775
hapmaprs863223775
1000 genomesrs863223775
hgdprs863223775
ensemblrs863223775
gopubmedrs863223775
geneviewrs863223775
scholarrs863223775
googlers863223775
pharmgkbrs863223775
gwascentralrs863223775
openSNPrs863223775
23andMers863223775
23andMe allrs863223775
SNP Nexus

SNPshotrs863223775
SNPdbers863223775
MSV3drs863223775
GWAS Ctlgrs863223775
Max Magnitude0
ClinVar
Risk rs863223775(T;T)
Alt rs863223775(T;T)
Reference rs863223775(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114836422G>A
CLNSRC
CLNACC RCV000198473.1,