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rs121434424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434424(A;A)
Make rs121434424(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position18869231
GeneGDF1, LASS1
is asnp
is mentioned by
dbSNPrs121434424
ebirs121434424
HLIrs121434424
Exacrs121434424
Varsomers121434424
Maprs121434424
PheGenIrs121434424
hapmaprs121434424
1000 genomesrs121434424
hgdprs121434424
ensemblrs121434424
gopubmedrs121434424
geneviewrs121434424
scholarrs121434424
googlers121434424
pharmgkbrs121434424
gwascentralrs121434424
openSNPrs121434424
23andMers121434424
23andMe allrs121434424
SNP Nexus

SNPshotrs121434424
SNPdbers121434424
MSV3drs121434424
GWAS Ctlgrs121434424
Max Magnitude0
OMIM602880
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434424(A;A)
Alt rs121434424(A;A)
Reference rs121434424(G;G)
Significance Pathogenic
Disease Tetralogy of Fallot not provided
Variation info
Gene CERS1 GDF1
CLNDBN Tetralogy of Fallot not provided
Reversed 1
HGVS NC_000019.9:g.18980040C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007141.3, RCV000180221.1,