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rs121434291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434291(A;A)
Make rs121434291(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position144414422
GeneSLC39A4
is asnp
is mentioned by
dbSNPrs121434291
ebirs121434291
HLIrs121434291
Exacrs121434291
Varsomers121434291
Maprs121434291
PheGenIrs121434291
hapmaprs121434291
1000 genomesrs121434291
hgdprs121434291
ensemblrs121434291
gopubmedrs121434291
geneviewrs121434291
scholarrs121434291
googlers121434291
pharmgkbrs121434291
gwascentralrs121434291
openSNPrs121434291
23andMers121434291
23andMe allrs121434291
SNP Nexus

SNPshotrs121434291
SNPdbers121434291
MSV3drs121434291
GWAS Ctlgrs121434291
Max Magnitude0
OMIM607059
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121434291(A;A)
Alt rs121434291(A;A)
Reference rs121434291(G;G)
Significance Pathogenic
Disease Hereditary acrodermatitis enteropathica
Variation info
Gene SLC39A4
CLNDBN Hereditary acrodermatitis enteropathica
Reversed 1
HGVS NC_000008.10:g.145639806C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003720.3,