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rs121434288

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434288(A;A)
Make rs121434288(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position144413288
GeneSLC39A4
is asnp
is mentioned by
dbSNPrs121434288
ebirs121434288
HLIrs121434288
Exacrs121434288
Varsomers121434288
Maprs121434288
PheGenIrs121434288
hapmaprs121434288
1000 genomesrs121434288
hgdprs121434288
ensemblrs121434288
gopubmedrs121434288
geneviewrs121434288
scholarrs121434288
googlers121434288
pharmgkbrs121434288
gwascentralrs121434288
openSNPrs121434288
23andMers121434288
23andMe allrs121434288
SNP Nexus

SNPshotrs121434288
SNPdbers121434288
MSV3drs121434288
GWAS Ctlgrs121434288
Max Magnitude0
OMIM607059
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121434288(A;A)
Alt rs121434288(A;A)
Reference rs121434288(G;G)
Significance Pathogenic
Disease Hereditary acrodermatitis enteropathica
Variation info
Gene SLC39A4
CLNDBN Hereditary acrodermatitis enteropathica
Reversed 1
HGVS NC_000008.10:g.145638672C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003716.3,