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rs869320763

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869320763(-;-)
Make rs869320763(-;C)
Make rs869320763(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position151424194
GenePOGZ
is asnp
is mentioned by
dbSNPrs869320763
ebirs869320763
HLIrs869320763
Exacrs869320763
Varsomers869320763
Maprs869320763
PheGenIrs869320763
hapmaprs869320763
1000 genomesrs869320763
hgdprs869320763
ensemblrs869320763
gopubmedrs869320763
geneviewrs869320763
scholarrs869320763
googlers869320763
pharmgkbrs869320763
gwascentralrs869320763
openSNPrs869320763
23andMers869320763
23andMe allrs869320763
SNP Nexus

SNPshotrs869320763
SNPdbers869320763
MSV3drs869320763
GWAS Ctlgrs869320763
Max Magnitude0
ClinVar
Risk rs869320763(C;C)
Alt rs869320763(C;C)
Reference rs869320763(;)
Significance Pathogenic
Disease White-sutton syndrome
Variation info
Gene POGZ
CLNDBN White-sutton syndrome
Reversed 1
HGVS NC_000001.10:g.151396671dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000210305.1,