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rs121909125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909125(C;T)
Make rs121909125(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position225937602
GeneLEFTY2
is asnp
is mentioned by
dbSNPrs121909125
ebirs121909125
HLIrs121909125
Exacrs121909125
Varsomers121909125
Maprs121909125
PheGenIrs121909125
hapmaprs121909125
1000 genomesrs121909125
hgdprs121909125
ensemblrs121909125
gopubmedrs121909125
geneviewrs121909125
scholarrs121909125
googlers121909125
pharmgkbrs121909125
gwascentralrs121909125
openSNPrs121909125
23andMers121909125
23andMe allrs121909125
SNP Nexus

SNPshotrs121909125
SNPdbers121909125
MSV3drs121909125
GWAS Ctlgrs121909125
Max Magnitude0
OMIM601877
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909125(T;T)
Alt rs121909125(T;T)
Reference rs121909125(C;C)
Significance Pathogenic
Disease Left-right axis malformations
Variation info
Gene LEFTY2
CLNDBN Left-right axis malformations
Reversed 1
HGVS NC_000001.10:g.226125302G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008078.2,