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rs137852953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852953(A;G)
Make rs137852953(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position166060066
GeneTLL1
is asnp
is mentioned by
dbSNPrs137852953
ebirs137852953
HLIrs137852953
Exacrs137852953
Varsomers137852953
Maprs137852953
PheGenIrs137852953
hapmaprs137852953
1000 genomesrs137852953
hgdprs137852953
ensemblrs137852953
gopubmedrs137852953
geneviewrs137852953
scholarrs137852953
googlers137852953
pharmgkbrs137852953
gwascentralrs137852953
openSNPrs137852953
23andMers137852953
23andMe allrs137852953
SNP Nexus

SNPshotrs137852953
SNPdbers137852953
MSV3drs137852953
GWAS Ctlgrs137852953
Max Magnitude0
OMIM606742
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852953(G;G)
Alt rs137852953(G;G)
Reference rs137852953(A;A)
Significance Pathogenic
Disease Atrial septal defect 6
Variation info
Gene TLL1
CLNDBN Atrial septal defect 6
Reversed 0
HGVS NC_000004.11:g.166981218A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004291.2,