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rs121434289

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434289(A;A)
Make rs121434289(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position144414291
GeneSLC39A4
is asnp
is mentioned by
dbSNPrs121434289
ebirs121434289
HLIrs121434289
Exacrs121434289
Varsomers121434289
Maprs121434289
PheGenIrs121434289
hapmaprs121434289
1000 genomesrs121434289
hgdprs121434289
ensemblrs121434289
gopubmedrs121434289
geneviewrs121434289
scholarrs121434289
googlers121434289
pharmgkbrs121434289
gwascentralrs121434289
openSNPrs121434289
23andMers121434289
23andMe allrs121434289
SNP Nexus

SNPshotrs121434289
SNPdbers121434289
MSV3drs121434289
GWAS Ctlgrs121434289
Max Magnitude0
OMIM607059
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121434289(A;A)
Alt rs121434289(A;A)
Reference rs121434289(G;G)
Significance Pathogenic
Disease Hereditary acrodermatitis enteropathica
Variation info
Gene SLC39A4
CLNDBN Hereditary acrodermatitis enteropathica
Reversed 1
HGVS NC_000008.10:g.145639675C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003717.3,