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rs28919570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28919570(C;T)
Make rs28919570(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position6816241
GeneCD4
is asnp
is mentioned by
dbSNPrs28919570
ebirs28919570
HLIrs28919570
Exacrs28919570
Varsomers28919570
Maprs28919570
PheGenIrs28919570
hapmaprs28919570
1000 genomesrs28919570
hgdprs28919570
ensemblrs28919570
gopubmedrs28919570
geneviewrs28919570
scholarrs28919570
googlers28919570
pharmgkbrs28919570
gwascentralrs28919570
openSNPrs28919570
23andMers28919570
23andMe allrs28919570
SNP Nexus

SNPshotrs28919570
SNPdbers28919570
MSV3drs28919570
GWAS Ctlgrs28919570
Max Magnitude0
ClinVar
Risk rs28919570(T;T)
Alt rs28919570(T;T)
Reference rs28919570(C;C)
Significance Pathogenic
Disease Okt4 epitope deficiency
Variation info
Gene CD4
CLNDBN Okt4 epitope deficiency
Reversed 0
HGVS NC_000012.11:g.6925407C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022781.23,