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rs121909126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909126(A;A)
Make rs121909126(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position225937517
GeneLEFTY2
is asnp
is mentioned by
dbSNPrs121909126
ebirs121909126
HLIrs121909126
Exacrs121909126
Varsomers121909126
Maprs121909126
PheGenIrs121909126
hapmaprs121909126
1000 genomesrs121909126
hgdprs121909126
ensemblrs121909126
gopubmedrs121909126
geneviewrs121909126
scholarrs121909126
googlers121909126
pharmgkbrs121909126
gwascentralrs121909126
openSNPrs121909126
23andMers121909126
23andMe allrs121909126
SNP Nexus

SNPshotrs121909126
SNPdbers121909126
MSV3drs121909126
GWAS Ctlgrs121909126
Max Magnitude0
OMIM601877
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909126(A;A)
Alt rs121909126(A;A)
Reference rs121909126(G;G)
Significance Pathogenic
Disease Left-right axis malformations
Variation info
Gene LEFTY2
CLNDBN Left-right axis malformations
Reversed 1
HGVS NC_000001.10:g.226125217C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008079.2,