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rs863223780

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223780(A;G)
Make rs863223780(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114401848
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223780
ebirs863223780
HLIrs863223780
Exacrs863223780
Varsomers863223780
Maprs863223780
PheGenIrs863223780
hapmaprs863223780
1000 genomesrs863223780
hgdprs863223780
ensemblrs863223780
gopubmedrs863223780
geneviewrs863223780
scholarrs863223780
googlers863223780
pharmgkbrs863223780
gwascentralrs863223780
openSNPrs863223780
23andMers863223780
23andMe allrs863223780
SNP Nexus

SNPshotrs863223780
SNPdbers863223780
MSV3drs863223780
GWAS Ctlgrs863223780
Max Magnitude0
ClinVar
Risk rs863223780(G;G)
Alt rs863223780(G;G)
Reference rs863223780(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114839653T>C
CLNSRC
CLNACC RCV000195628.1,