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rs137852954

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852954(C;G)
Make rs137852954(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position35248766
GeneTBX20
is asnp
is mentioned by
dbSNPrs137852954
ebirs137852954
HLIrs137852954
Exacrs137852954
Varsomers137852954
Maprs137852954
PheGenIrs137852954
hapmaprs137852954
1000 genomesrs137852954
hgdprs137852954
ensemblrs137852954
gopubmedrs137852954
geneviewrs137852954
scholarrs137852954
googlers137852954
pharmgkbrs137852954
gwascentralrs137852954
openSNPrs137852954
23andMers137852954
23andMe allrs137852954
SNP Nexus

SNPshotrs137852954
SNPdbers137852954
MSV3drs137852954
GWAS Ctlgrs137852954
Max Magnitude0
OMIM606061
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852954(A,G;A,G)
Alt rs137852954(A,G;A,G)
Reference rs137852954(C;C)
Significance Pathogenic
Disease Atrial septal defect 4
Variation info
Gene TBX20
CLNDBN Atrial septal defect 4
Reversed 1
HGVS NC_000007.13:g.35288378G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004895.2,