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rs1057518199

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518199(-;-)
Make rs1057518199(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position114401866
GeneTBX5
is asnp
is mentioned by
dbSNPrs1057518199
dbSNP (classic)rs1057518199
ClinGenrs1057518199
ebirs1057518199
HLIrs1057518199
Exacrs1057518199
Gnomadrs1057518199
Varsomers1057518199
LitVarrs1057518199
Maprs1057518199
PheGenIrs1057518199
Biobankrs1057518199
1000 genomesrs1057518199
hgdprs1057518199
ensemblrs1057518199
geneviewrs1057518199
scholarrs1057518199
googlers1057518199
pharmgkbrs1057518199
gwascentralrs1057518199
openSNPrs1057518199
23andMers1057518199
23andMe allrs1057518199
SNPshotrs1057518199
SNPdbers1057518199
MSV3drs1057518199
GWAS Ctlgrs1057518199
Max Magnitude0
ClinVar
Risk rs1057518199(-;-)
Alt rs1057518199(-;-)
Reference Rs1057518199(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114839671delG
CLNSRC
CLNACC RCV000413997.1,