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rs879255404

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255404(C;T)
Make rs879255404(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position151405776
GenePOGZ
is asnp
is mentioned by
dbSNPrs879255404
ebirs879255404
HLIrs879255404
Exacrs879255404
Varsomers879255404
Maprs879255404
PheGenIrs879255404
hapmaprs879255404
1000 genomesrs879255404
hgdprs879255404
ensemblrs879255404
gopubmedrs879255404
geneviewrs879255404
scholarrs879255404
googlers879255404
pharmgkbrs879255404
gwascentralrs879255404
openSNPrs879255404
23andMers879255404
23andMe allrs879255404
SNP Nexus

SNPshotrs879255404
SNPdbers879255404
MSV3drs879255404
GWAS Ctlgrs879255404
Max Magnitude0
ClinVar
Risk rs879255404(T;T)
Alt rs879255404(T;T)
Reference rs879255404(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151378252G>A
CLNSRC
CLNACC RCV000238773.1,