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rs1057517833

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517833(C;T)
Make rs1057517833(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position114385561
GeneTBX5
is asnp
is mentioned by
dbSNPrs1057517833
dbSNP (old)rs1057517833
ClinGenrs1057517833
ebirs1057517833
HLIrs1057517833
Exacrs1057517833
Gnomadrs1057517833
Varsomers1057517833
Maprs1057517833
PheGenIrs1057517833
Biobankrs1057517833
1000 genomesrs1057517833
hgdprs1057517833
ensemblrs1057517833
gopubmedrs1057517833
geneviewrs1057517833
scholarrs1057517833
googlers1057517833
pharmgkbrs1057517833
gwascentralrs1057517833
openSNPrs1057517833
23andMers1057517833
23andMe allrs1057517833
SNPshotrs1057517833
SNPdbers1057517833
MSV3drs1057517833
GWAS Ctlgrs1057517833
Max Magnitude0
ClinVar
Risk rs1057517833(T;T)
Alt rs1057517833(T;T)
Reference Rs1057517833(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114823366G>A
CLNSRC
CLNACC RCV000413700.1,