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rs778210210

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778210210(C;G)
Make rs778210210(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position102344551
GeneSLC39A8
is asnp
is mentioned by
dbSNPrs778210210
ebirs778210210
HLIrs778210210
Exacrs778210210
Varsomers778210210
Maprs778210210
PheGenIrs778210210
hapmaprs778210210
1000 genomesrs778210210
hgdprs778210210
ensemblrs778210210
gopubmedrs778210210
geneviewrs778210210
scholarrs778210210
googlers778210210
pharmgkbrs778210210
gwascentralrs778210210
openSNPrs778210210
23andMers778210210
23andMe allrs778210210
SNP Nexus

SNPshotrs778210210
SNPdbers778210210
MSV3drs778210210
GWAS Ctlgrs778210210
Max Magnitude0
ClinVar
Risk rs778210210(G;G)
Alt rs778210210(G;G)
Reference rs778210210(C;C)
Significance Pathogenic
Disease CONGENITAL DISORDER OF GLYCOSYLATION SLC39A8 deficiency
Variation info
Gene SLC39A8
CLNDBN CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn SLC39A8 deficiency
Reversed 0
HGVS NC_000004.11:g.103265708C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000203234.1, RCV000203261.1,