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rs137852955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852955(C;T)
Make rs137852955(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position35245020
GeneTBX20
is asnp
is mentioned by
dbSNPrs137852955
ebirs137852955
HLIrs137852955
Exacrs137852955
Varsomers137852955
Maprs137852955
PheGenIrs137852955
hapmaprs137852955
1000 genomesrs137852955
hgdprs137852955
ensemblrs137852955
gopubmedrs137852955
geneviewrs137852955
scholarrs137852955
googlers137852955
pharmgkbrs137852955
gwascentralrs137852955
openSNPrs137852955
23andMers137852955
23andMe allrs137852955
SNP Nexus

SNPshotrs137852955
SNPdbers137852955
MSV3drs137852955
GWAS Ctlgrs137852955
Max Magnitude0
OMIM606061
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852955(T;T)
Alt rs137852955(T;T)
Reference rs137852955(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.35284632G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004896.2,