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rs864321672

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864321672(-;C)
Make rs864321672(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151406271
GenePOGZ
is asnp
is mentioned by
dbSNPrs864321672
ClinGenrs864321672
ebirs864321672
HLIrs864321672
Exacrs864321672
Varsomers864321672
Maprs864321672
PheGenIrs864321672
hapmaprs864321672
1000 genomesrs864321672
hgdprs864321672
ensemblrs864321672
gopubmedrs864321672
geneviewrs864321672
scholarrs864321672
googlers864321672
pharmgkbrs864321672
gwascentralrs864321672
openSNPrs864321672
23andMers864321672
23andMe allrs864321672
SNP Nexus

SNPshotrs864321672
SNPdbers864321672
MSV3drs864321672
GWAS Ctlgrs864321672
Max Magnitude0
ClinVar
Risk rs864321672(C;C)
Alt rs864321672(C;C)
Reference Rs864321672(;)
Significance Pathogenic
Disease White-sutton syndrome
Variation info
Gene POGZ
CLNDBN White-sutton syndrome
Reversed 1
HGVS NC_000001.10:g.151378748dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000203509.1,