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rs863223785

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAAACTCAAGCTCACCA;GAAACTCAAGCTCACCA) 0 common in clinvar
Make rs863223785(-;-)
Make rs863223785(-;GAAACTCAAGCTCACCA)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position114398599
GeneTBX5
is asnp
is mentioned by
dbSNPrs863223785
dbSNP (classic)rs863223785
ClinGenrs863223785
ebirs863223785
HLIrs863223785
Exacrs863223785
Gnomadrs863223785
Varsomers863223785
LitVarrs863223785
Maprs863223785
PheGenIrs863223785
Biobankrs863223785
1000 genomesrs863223785
hgdprs863223785
ensemblrs863223785
geneviewrs863223785
scholarrs863223785
googlers863223785
pharmgkbrs863223785
gwascentralrs863223785
openSNPrs863223785
23andMers863223785
SNPshotrs863223785
SNPdbers863223785
MSV3drs863223785
GWAS Ctlgrs863223785
Max Magnitude0
ClinVar
Risk rs863223785(-;-)
Alt rs863223785(-;-)
Reference Rs863223785(GAAACTCAAGCTCACCA;GAAACTCAAGCTCACCA)
Significance Pathogenic
Disease not provided
Variation info
Gene TBX5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.114836404_114836420del17
CLNSRC
CLNACC RCV000196710.1,