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rs863223778

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223778(C;T)
Make rs863223778(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114355963
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223778
ebirs863223778
HLIrs863223778
Exacrs863223778
Varsomers863223778
Maprs863223778
PheGenIrs863223778
hapmaprs863223778
1000 genomesrs863223778
hgdprs863223778
ensemblrs863223778
gopubmedrs863223778
geneviewrs863223778
scholarrs863223778
googlers863223778
pharmgkbrs863223778
gwascentralrs863223778
openSNPrs863223778
23andMers863223778
23andMe allrs863223778
SNP Nexus

SNPshotrs863223778
SNPdbers863223778
MSV3drs863223778
GWAS Ctlgrs863223778
Max Magnitude0
ClinVar
Risk rs863223778(T;T)
Alt rs863223778(T;T)
Reference rs863223778(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114793768G>A
CLNSRC
CLNACC RCV000197304.2,