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rs863223776

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223776(A;A)
Make rs863223776(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114385476
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223776
ebirs863223776
HLIrs863223776
Exacrs863223776
Varsomers863223776
Maprs863223776
PheGenIrs863223776
hapmaprs863223776
1000 genomesrs863223776
hgdprs863223776
ensemblrs863223776
gopubmedrs863223776
geneviewrs863223776
scholarrs863223776
googlers863223776
pharmgkbrs863223776
gwascentralrs863223776
openSNPrs863223776
23andMers863223776
23andMe allrs863223776
SNP Nexus

SNPshotrs863223776
SNPdbers863223776
MSV3drs863223776
GWAS Ctlgrs863223776
Max Magnitude0
ClinVar
Risk rs863223776(A;A)
Alt rs863223776(A;A)
Reference rs863223776(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114823281C>T
CLNSRC
CLNACC RCV000198982.1,