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rs863223779

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223779(A;A)
Make rs863223779(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114401853
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223779
ebirs863223779
HLIrs863223779
Exacrs863223779
Varsomers863223779
Maprs863223779
PheGenIrs863223779
hapmaprs863223779
1000 genomesrs863223779
hgdprs863223779
ensemblrs863223779
gopubmedrs863223779
geneviewrs863223779
scholarrs863223779
googlers863223779
pharmgkbrs863223779
gwascentralrs863223779
openSNPrs863223779
23andMers863223779
23andMe allrs863223779
SNP Nexus

SNPshotrs863223779
SNPdbers863223779
MSV3drs863223779
GWAS Ctlgrs863223779
Max Magnitude0
ClinVar
Risk rs863223779(A;A)
Alt rs863223779(A;A)
Reference rs863223779(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114839658G>T
CLNSRC
CLNACC RCV000198872.1,