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rs121434289

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;G) 3 Carrier of an acrodermatitis enteropathica mutation
(G;G) 0 common in complete genomics


Make rs121434289(A;A)
ReferenceGRCh38 38.1/141
Chromosome8
Position144414291
GeneSLC39A4
is asnp
is mentioned by
dbSNPrs121434289
dbSNP (classic)rs121434289
ClinGenrs121434289
ebirs121434289
HLIrs121434289
Exacrs121434289
Gnomadrs121434289
Varsomers121434289
LitVarrs121434289
Maprs121434289
PheGenIrs121434289
Biobankrs121434289
1000 genomesrs121434289
hgdprs121434289
ensemblrs121434289
geneviewrs121434289
scholarrs121434289
googlers121434289
pharmgkbrs121434289
gwascentralrs121434289
openSNPrs121434289
23andMers121434289
SNPshotrs121434289
SNPdbers121434289
MSV3drs121434289
GWAS Ctlgrs121434289
Max Magnitude3

aka c.1120G>A (p.Gly374Arg)

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,