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rs864321675

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864321675(-;T)
Make rs864321675(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151406254
GenePOGZ
is asnp
is mentioned by
dbSNPrs864321675
ClinGenrs864321675
ebirs864321675
HLIrs864321675
Exacrs864321675
Varsomers864321675
Maprs864321675
PheGenIrs864321675
hapmaprs864321675
1000 genomesrs864321675
hgdprs864321675
ensemblrs864321675
gopubmedrs864321675
geneviewrs864321675
scholarrs864321675
googlers864321675
pharmgkbrs864321675
gwascentralrs864321675
openSNPrs864321675
23andMers864321675
23andMe allrs864321675
SNP Nexus

SNPshotrs864321675
SNPdbers864321675
MSV3drs864321675
GWAS Ctlgrs864321675
Max Magnitude0
ClinVar
Risk rs864321675(T;T)
Alt rs864321675(T;T)
Reference Rs864321675(-;-)
Significance Pathogenic
Disease White-sutton syndrome
Variation info
Gene POGZ
CLNDBN White-sutton syndrome
Reversed 1
HGVS NC_000001.10:g.151378731dupA
CLNSRC
CLNACC RCV000203581.1,