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rs121434293

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434293(C;C)
Make rs121434293(C;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position144414792
GeneSLC39A4
is asnp
is mentioned by
dbSNPrs121434293
ebirs121434293
HLIrs121434293
Exacrs121434293
Varsomers121434293
Maprs121434293
PheGenIrs121434293
hapmaprs121434293
1000 genomesrs121434293
hgdprs121434293
ensemblrs121434293
gopubmedrs121434293
geneviewrs121434293
scholarrs121434293
googlers121434293
pharmgkbrs121434293
gwascentralrs121434293
openSNPrs121434293
23andMers121434293
23andMe allrs121434293
SNP Nexus

SNPshotrs121434293
SNPdbers121434293
MSV3drs121434293
GWAS Ctlgrs121434293
Max Magnitude0
OMIM607059
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121434293(C;C)
Alt rs121434293(C;C)
Reference rs121434293(G;G)
Significance Pathogenic
Disease Hereditary acrodermatitis enteropathica
Variation info
Gene SLC39A4
CLNDBN Hereditary acrodermatitis enteropathica
Reversed 1
HGVS NC_000008.10:g.145640176C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003723.3,