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rs863223777

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223777(C;T)
Make rs863223777(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114403757
GeneLOC105369997, TBX5
is asnp
is mentioned by
dbSNPrs863223777
ebirs863223777
HLIrs863223777
Exacrs863223777
Varsomers863223777
Maprs863223777
PheGenIrs863223777
hapmaprs863223777
1000 genomesrs863223777
hgdprs863223777
ensemblrs863223777
gopubmedrs863223777
geneviewrs863223777
scholarrs863223777
googlers863223777
pharmgkbrs863223777
gwascentralrs863223777
openSNPrs863223777
23andMers863223777
23andMe allrs863223777
SNP Nexus

SNPshotrs863223777
SNPdbers863223777
MSV3drs863223777
GWAS Ctlgrs863223777
Max Magnitude0
ClinVar
Risk rs863223777(T;T)
Alt rs863223777(T;T)
Reference rs863223777(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC101928456 TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114841562G>A
CLNSRC
CLNACC RCV000200559.2,