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rs121434363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434363(A;A)
Make rs121434363(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47410315
GeneSLC39A13
is asnp
is mentioned by
dbSNPrs121434363
ebirs121434363
HLIrs121434363
Exacrs121434363
Varsomers121434363
Maprs121434363
PheGenIrs121434363
hapmaprs121434363
1000 genomesrs121434363
hgdprs121434363
ensemblrs121434363
gopubmedrs121434363
geneviewrs121434363
scholarrs121434363
googlers121434363
pharmgkbrs121434363
gwascentralrs121434363
openSNPrs121434363
23andMers121434363
23andMe allrs121434363
SNP Nexus

SNPshotrs121434363
SNPdbers121434363
MSV3drs121434363
GWAS Ctlgrs121434363
Max Magnitude0
OMIM608735
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434363(A;A)
Alt rs121434363(A;A)
Reference rs121434363(G;G)
Significance Pathogenic
Disease Spondylocheirodysplasia
Variation info
Gene SLC39A13
CLNDBN Spondylocheirodysplasia, Ehlers-Danlos syndrome-like
Reversed 0
HGVS NC_000011.9:g.47431866G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002215.2,